cbd oil for seborrheic dermatitis

Efficacy and Tolerability of a Shampoo Containing Broad-Spectrum Cannabidiol in the Treatment of Scalp Inflammation in Patients with Mild to Moderate Scalp Psoriasis or Seborrheic Dermatitis

Scalp inflammation is commonly associated with scalp psoriasis or seborrheic dermatitis. It can aggravate the progression of androgenetic alopecia and cause troublesome itching and burning. Here, we evaluate the efficacy of a shampoo containing 0.075% broad-spectrum cannabidiol in 50 subjects with mild to moderate scalp psoriasis or seborrheic dermatitis.


Inflammation was assessed by evaluating the density of twisted/glomerular or arborizing vessels by trichoscopy using a 6-point scale at baseline and day 14. Symptoms of itching/burning sensation, clinical evaluation of erythema/scaling, overall tolerability, and subject satisfaction were evaluated using 10-point scales.


There were significant reductions in arborizing vessel/twisted capillary inflammation and scaling by day 14. Severity scores reduced from 2.3 ± 0.1, 2.6 ± 0.1, and 3.6 ± 0.1, respectively, to 0.5 ± 0.05, 0.8 ± 0.05, and 0.6 ± 0.05 (all p < 0.0001). Symptom scores of itching and burning also reduced significantly from 6.9 ± 0.1 to 4.5 ± 0.1 to 1.5 ± 0.05 and 1.0 ± 0.05 (both p < 0.0001). Severity of erythema and scaling was also significantly reduced from 5.5 ± 0.1 and 7.0 ± 0.1, respectively, to 1.3 ± 0.05 and 1.6 ± 0.05 (both p < 0.0001). Tolerability and subject satisfaction were both excellent. There were no significant differences in treatment effect, tolerability, or subject satisfaction between men and women.


Replacing current shampooing practices with a broad-spectrum cannabidiol-containing shampoo significantly reduces both severity and symptoms of scalp inflammation within 2 weeks, with excellent tolerability and treatment satisfaction in subjects with mild to moderate scalp psoriasis or seborrheic dermatitis.


Oxidative stress and scalp inflammation cause telogen effluvium, which affects the health of the follicle and could trigger and aggravate progression of androgenetic alopecia [1, 2, 3, 4].

Scalp inflammation is commonly associated with scalp psoriasis or seborrheic dermatitis (SD). Scalp psoriasis can be a cause of significant physical and social distress, with 97% of affected individuals reporting interference with their daily lives [5]. Patients are often symptomatic and complain of itching and burning [6]. Itching was identified as the most bothersome symptom in 43% of respondents to a telephone survey [7]. Hair loss is also very common in the author’s experience.

Psoriasis is also a very common skin disease. Although women generally have less severe psoriasis than men, specifically in scalp psoriasis severity is similar, perhaps due to gender-specific differences in hair growth care and styling [8]. SD is one of the most common inflammatory dermatoses in middle-aged people and is particularly prevalent in men and people with light and dry skin [9].

Trichoscopy is proven to be a noninvasive, cost-effective, and useful diagnostic method to assess the severity of inflammatory changes in these conditions. In scalp psoriasis, trichoscopy shows red dots at low magnification and twisted/glomerular capillary loops at higher magnifications [10]. In SD, it shows an increased number of arborizing vessels [11]. Here, we use trichoscopic evaluation of the scalp to assess the efficacy of an anti-inflammatory shampoo (Revita;CBD, DS Laboratories) in treating scalp inflammation due to mild/moderate scalp psoriasis or SD. In addition to a number of ingredients known to have beneficial effects in scalp conditions (ketoconazole, rooibos tea, taurine, caffeine, apple polyphenol, cysteine, spin traps, carnitine tartrate, biotin, ornithine, emu oil, methylsulfonylmethane, and ornithine), the shampoo contains as its main ingredient the phytocannabinoid, (−)-cannabidiol (CBD), which exerts sebostatic and anti-inflammatory effects on the pilosebaceous unit [12].


Before initiating the study, subjects were required to give written consent. Subjects who met the inclusion criteria were eligible for the study. The inclusion criteria were those of either gender, aged 18–65 years, with mild to moderate scalp psoriasis or SD. Severity of disease was established through clinical evaluation of scaling and erythema and subjective assessment of symptoms of itching and burning. The exclusion criteria were scarring alopecia, alopecia areata, pregnancy/breast feeding, history of hair transplant, and a known allergy or sensitivity to the study medication or any of its components.

Trichoscopic evaluation of the scalp to assess inflammation was undertaken with a video dermatoscope (FotoFinder Systems GmbH, Bad Birnbach, Germany), with ×20 and ×50 magnification photographs, using a 6-point scale where 0 = ≤10, 1 = 10–25, 2 = 25–50, 3 = 50–75, 4 = 75–100, and 5 = 100% of the involved field of dermoscopy patient images for arborizing vessels, twisted capillaries, and scales as described previously [13]. Clinical evaluation of scaling and erythema utilized a 10-point scale (where 1 = none).

Subjects provided an insight into symptoms of itching and burning by answering a number of questions. Their overall severity of itching and burning was assessed using a 10-point scale (where 1 = none). Subsequent reduction of itching and burning was also assessed using a 7-point scale (where −3 = great decrease and +3 = great increase).

Subjects were instructed to use the study shampoo over a 14-day period without changing their shampooing frequency. Changes in disease and symptom severity were again assessed at the end of the study.

In addition, the subjects were assessed for tolerability and treatment satisfaction using a 10-point subjective scale. The subjects were asked how satisfied they were with therapy, and their views on treatment attributes such as smell, consistency, and ease of application using a similar scale. Gender data were also analyzed.

Statistical Analysis

Data are presented as mean ± SEM. Comparisons between groups were made using Student’s t test. GraphPad Prism 6 software for OSX was used to run the analysis. Differences were considered significant at p ≤ 0.05.


Participants in the study comprised 24 males and 26 females, aged 18–61 years (mean age 38 and 46 years, respectively). Seven subjects were categorized as mild and 43 subjects as moderate disease. Twenty-two subjects had scalp psoriasis and 28 subjects SD.

At baseline, the mean severity scores for arborizing vessels, twisted capillaries, and scales were 2.3 ± 0.1, 2.6 ± 0.1, and 3.6 ± 0.1, respectively. The mean severity scores for erythema and scaling were 5.5 ± 0.1 and 7.0 ± 0.1, respectively. Subjective assessment scores for itching and burning at baseline were 6.9 ± 0.1 and 4.5 ± 0.1, respectively.

Following 2 weeks’ treatment with the study shampoo, severity scores for arborizing vessels, twisted capillaries, and scales reduced to 0.5 ± 0.05, 0.8 ± 0.05, and 0.6 ± 0.05, respectively (Fig. ​ (Fig.1: 1 : all p < 0.0001). Severity scores for erythema and scaling reduced to 1.3 ± 0.05 and 1.6 ± 0.05, respectively (Fig. ​ (Fig.2: 2 : both p < 0.0001).

Effect on mean scores (SEM) following 2 weeks’ treatment. Scores for arborizing vessels, twisted capillary, and scales assessed by videodermoscopy. ***p < 0.0001.

Clinical evaluation. Effect on mean scores (SEM) of erythema and scaling following 2 weeks’ treatment. Scores using a 10-point scale. ***p < 0.0001.

Scores for itching and burning at week 2 were 1.5 ± 0.05 and 1.0 ± 0.05, respectively (both p < 0.0001). The mean scores for the reduction in itching and burning were 2.7 ± 0.05 and 2.7 ± 0.05, respectively, where 2 = moderate reduction and 3 = great reduction (Fig. ​ (Fig.3). 3 ). Subject assessment mean scores for tolerability and overall satisfaction at the end of the study were both 9.0 (Fig. ​ (Fig.4: 4 : range 7–10). There were no side effects reported. The mean scores for smell, consistency, and ease of application were 8.7, 8.1, and 9.2, respectively (out of a maximum score of 10). Representative examples of the efficacy of the study shampoo are shown in Figure ​ Figure5 5 .

Subject self-assessment. Effect on mean scores (SEM) for itching and burning following 2 weeks’ treatment and reduction in itching/burning. Scores using the 10-point scale and reduction assessed using the 7-point scale. ***p < 0.0001.

Tolerability and subject satisfaction at week 2. Scores using the 10-point scale.

Representative examples of efficacy of study shampoo using videodermoscopy in subjects with SD (a, b) and scalp psoriasis (c, d) (×20 magnification). SD, seborrheic dermatitis.

Gender Assessment

At baseline, disease severity as assessed by dermoscopy was similar in males (mean scores for arborizing vessels, twisted capillaries, and scales of 1.2, 1.2, and 1.8, respectively) compared with 1.0, 1.4, and 1.8, respectively, in females. Clinical evaluation of erythema and scaling was also similar (mean scores 2.7 and 3.4 vs. 2.8 and 3.6, respectively). Subject assessment scores for itching and burning were slightly higher in females (mean scores 3.3 and 2.1 vs. 3.6 and 2.4, respectively).

At week 2, the benefits of treatment were similar across gender (Fig. ​ (Fig.6). 6 ). There were no significant gender differences in terms of reduction in itching or burning, tolerability, or subject satisfaction.

Gender differences in efficacy, tolerability, and subject satisfaction as assessed by videodermoscopy, clinical evaluation, and subject evaluation. *p < 0.01, ***p < 0.0001.


Scalp psoriasis and SD are both very common dermatoses, with significant distress and impaired quality of life. Psoriasis of the scalp presents earlier and more frequently than that of other sites, with itching being the most bothersome symptom affecting every patient to some degree. There is a positive correlation between the severity of the lesions and itch [14]. SD, which affects approximately 16% of the adult population, is the most common cause of scalp itching. Both conditions can cause telogen effluvium and accelerate progression of androgenetic alopecia.

The diseases can be distinguished using trichoscopy [15]. Patients with scalp psoriasis present with red dots at low magnification and twisted/glomerular vessels at high magnification. Additional features include red loops, hairpin vessels, white scales, and punctate hemorrhages. In patients with SD, trichoscopy shows an increased number of arborizing vessels. They both represent pathologic conditions in which oxidative stress and inflammation are commonly detected [1]. The inflammatory process in SD is mediated by fungal metabolites from Malassezia spp. [16], specifically free fatty acids released from triglycerides. There are clear signs of oxidative stress as indicated by perturbed surface and systemic antioxidant enzyme levels [17] and observations from surface samples of elevated lipid peroxidation [18]. Overgrowth of the scalp with Malassezia spp. has also been described in scalp psoriasis [19]. Indicators of oxidative stress in psoriasis include antioxidant enzymes [20], oxidized proteins [21, 22], and oxidized lipids [23].

Shampoo treatments are the most commonly used means of managing hair and scalp conditions and have proven to be effective in the treatment of psoriasis [2] and SD [24, 25, 26]. They exert their benefits through controlling scalp Malassezia levels, and the resultant oxidative stress and inflammation [27].

Here, we studied the efficacy and tolerability of a shampoo uniquely formulated using a number of synergistic ingredients known to have benefits in subjects with mild to moderate scalp psoriasis or SD using trichoscopy as well as subjective and objective assessments of changes in symptoms. The shampoo ingredients include ketoconazole [28, 29] which reduces Malassezia spp., numerous ingredients that promote hair growth [30, 31], and a broad-spectrum CBD, which was added to the formulation for its anti-inflammatory effects on the pilosebaceous unit and potential to reduce oxidative stress. Cannabidiol is immunosuppressive for various immune cell types, inducing apoptosis and promotion of regulatory cells, which control other immune cell targets [32]. It reduces the expression of nitrotyrosine (iNOS) in different tissues suggesting they may be responsible for the reduction of cytokine production, counteracting the rise in iNOS levels and the downstream cascade of events triggered by the inflammatory process, and reducing oxidative stress [33]. They also inhibit lymphocyte proliferation and the production of interleukin-2 (IL-2), interferon-c, IL-1a, IL-1b, and tumor necrosis factor-alpha.

The interaction between the anti-inflammatory pathway and the endocannabinoid system suggests a role for cannabinoids in treating psoriasis [34]. Cannabidiol can exert a suppressive effect on human keratinocyte proliferation [35, 36]. The antiproliferative and anti-inflammatory effects of CBD could be associated with specific sebostatic actions. It normalizes the pathologically elevated lipogenesis, suppresses cell proliferation, and prevents the actions of toll-like receptor activation that elevates proinflammatory cytokine levels [12]. Cannabidiol may inhibit the enzyme 5-α-reductase, subsequently inhibiting excessive skin sebum secretion and improving skin elasticity and hydration. Cannabidiol has high lipophilicity that helps it to reach and accumulate in the sebaceous glands through transfollicular delivery, having a therapeutic effect hours after applying the product [12].

In our study, the study shampoo containing a broad-spectrum CBD was shown to be highly effective in reducing signs of scalp inflammation (arborizing vessels, twisted capillaries, and scales), as well as reducing symptoms of erythema and scaling, itching, and burning, following 2 weeks’ use. Baseline severity was similar in males and females, and there was no significant gender difference in terms of reduction in itching and burning, tolerability, or subject satisfaction in males or females.

In conclusion, replacing current shampooing practices with a broad-spectrum cannabidiol-containing shampoo significantly reduces both severity and symptoms of scalp inflammation within 2 weeks, with excellent tolerability and treatment satisfaction in subjects with mild to moderate scalp psoriasis or SD.

Statement of Ethics

The EU guidelines on IRB approval (reinforced by Italian law regarding tests on human beings) exclude from IRB approval cosmetic testing as mentioned in section 1.2.9 of the Official Journal of EU (March 30, 2010). Anyway, we committed ourselves to the safeguard of the rights and well-being of all the trial subjects by following the principles of the Helsinki Declaration and letting them know all the relevant aspects of their participation through a written informed consent.

Conflict of Interest Statement

Dr. Vincenzi has no conflicts; Dr. Tosti is a consultant for DS Healthcare Group, Monat Global, Almirall, Thirty Madison, Lilly, Leo Pharmaceuticals, Bristol Myers Squibb, and P&G.

Funding Sources

The study was funded by a grant from DS Laboratories.

Author Contributions

Dr. Vincenzi: collection and organization of data, and drafting of manuscript. Dr. Tosti: study protocol, revision of data, and final manuscript.

This CBD Oil Saved My Skin From Full Blown Painful Itchiness

It started when I was about 14. The sides of my nose got really red. Then they got flaky. Then they got weepy. Then I got weepy. I didn’t love it. But I also had no recourse to address it, let alone fix it. I didn’t want to draw attention to it, so I just ignored my own face in the hopes that it would fix itself. Once that was no longer an option, I went to the doctor.

I had seborrheic dermatitis, which is kind of like dandruff but red and scaly and on your face. Love that for me! I was quickly given a lotion whose only ingredients were sulfur and mineral oils, and sent on my way. In the years that followed, I treated seasonal and stress-related flare ups with soap-free face wash, cortisone cream, and that’s pretty much it. The idea of using a daily moisturizer—let alone an all-out face oil—was terrifying to my uneducated brain. My motto was pretty much “Don’t touch it!!”

In the last few years, however, I’ve become acquainted with a little concept called clean beauty and rose hydrosol and 100 percent argan oil have become my new best friends. I’ve been able to slowly decrease applications of the aforementioned medical lotion, as my new skincare regimen keeps my overactive sebum production in check. For the most part. Flare ups still happen. That’s where CBD comes in.

As you can imagine, working at Miss Grass has meant CBD has infused itself into almost all aspects of my life. But only now, having been enabled by our ecommerce manager, have I tried incorporating a high-strength CBD oil into my daily skincare regimen. And not just any CBD oil.

I’m talking about the luxe leaders of CBD and skin, Lord Jones. I’m talking about their most potent product yet; their Royal Oil. I set myself the task of using it every day—as a facial oil and as a tincture—and this (not to be dramatic) is my story.

Why Even?

Like everything related to cannabis, some initial research into the efficacy of CBD as a treatment for skin buggers like dermatitis as yielded promising results, but there’s not enough studies at this point to know why, when, and how it all works. Generally speaking, managing skin issues via the endocannabinoid system (ECS) makes sense.

After all, the skin that covers our bods has a functioning ECS going on, right there. Which makes sense, given the skin’s role in maintaining homeostasis and acting as the vanguard of the human body in fighting off injury and infection.

The superstar endocannabinoid receptors, CB1 and CB2, are present in practically all cell types of the skin, too. These guys help prevent inflammation, and with some help from CBD, they have the potential to do a lot more. One study from Nottingham University points to the potential for CBD to play a role in the slowing down of the proliferation of skin cells linked to skin like mine. Another 2014 study published in the journal of the American Society for Clinical Investigation proposed that CBD also slows down the secretion of sebum a.k.a. literally the cause of seborrheic dermatitis.

Having researched the above, and with all signs pointing to promising, I set about covering my face in CBD oil at any opportunity. And at 1000mg of CBD per 30ml bottle of Royal Oil, that was a lot of CBD.

My (New) Royal Regimen

The potency of Royal Oil is what it’s known for, as you can imagine. Each full dropper contains about 40ml of CBD. Normally, that’d be enough to get a lightweight with no prior CBD experience a little fuzzy-headed. But Lord Jones products contain broad spectrum CBD; they contain all the natural cannabinoids and terpenes, minus the trace amounts of psychoactive THC. So even if you drank the whole bottle (please don’t) you wouldn’t be a trace high.

But back to my skin. It responds much better to all-natural ingredients, it turns out. And for skin care purists, you’ll be pleased to know that Royal Oil contains two essential ingredients; broad spectrum CBD suspended in grape seed oil. No flavorings, colors, or additives—just a subtle, gorgeous cannabis scent.

Having stalked the Sephora reviews for Royal Oil to compare my experience, it seems that some people have found applying ample amounts of grape seed oil to their face causes them to break out. Not to brag, but I’m not one of those people. It’s been almost two weeks and I have the same amount of pimples I always do. Which is average. If anything, that amount’s dropped slightly—no small feat considering my experimentation overlapped with the onset of my period.

How’s the dermatitis, you ask? Zero flare ups. At one point about a week ago, I found I was developing some related dryness on my neck. I slapped it with Royal Oil each night before bed (the only time face oils should be applied, by the way) and after three or four nights? It calmed all the way down to non-existent status. And considering that means it went all the way from red and scaly, to straight up my-skin-color and smooth, that’s kind of a big deal.

But my favorite part of using Royal Oil is the ritual of a multipurpose CBD oil with such potency. In the mornings, I would drop some into my AM beverage (a protein drink, most days) and at night, I would put a dropper’s worth under my tongue and another on my face after cleansing and hydrosol spritzing. Then I would jade roll that shit right into my epidermis with all the tenderness and self-love I could muster.

Yes, I’m describing all of this in past tense, but believe me: I’ll be doing this exact same thing with this exact product for the rest of my life. At least while I have a Miss Grass staff discount code. Because at $100 a pop, it’s an investment for sure. But hey, this is your largest organ we’re talking about.