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Based on scientific evidence the following approaches have shown
to be effective. To review the supporting scientific evidence, select
a treatment option.
Ayurveda
Biofeedback
Herbal Medicine
Nutrition/Supplementation
In order to help interpret the strength of the scientific evidence (the
level of proof) provided, descriptions of the different types of
studies, reviews and guidelines are available in the glossary.
Please click on each term for a discussion of the topic: Case
review, consensus
statement, controlled
clinical trial, guidelines
and recommendations, literature
review, meta-analysis,
multi-center study,
outcome study, systematic
review.
Ayurveda
Author(s):
Paranjpe P, Kulkarni PH
Institution:
Acne Clinic, Nanal Hospital, India
Title:
Comparative efficacy of four Ayurvedic formulations in the treatment of acne vulgaris: a double-blind randomised placebo-controlled clinical evaluation
Source:
Journal of Ethnopharmacology. 49(3)127-32, 1995
Type of study:
randomized placebo-controlled clinical trial
Control/comparison:
placebo
Sample characteristics:
82 patients with acne
Type of intervention:
4 different Ayurvedic treatments given orally for 6 weeks
Primary outcome measure(s):
clinical investigations and lesion count were carried out at 2 week intervals
Outcome:
A significant reduction in lesion count was observed in patients receiving Sundar Vati
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Biofeedback
Author(s):
Hughes H, Brown BW, Lawlis GF, et al.
Institution:
Department of Psychology, North Texas State University, Denton, TX
Title:
Treatment of acne vulgaris by biofeedback relaxation and cognitive imagery
Source:
Journal of Psychosomatic Research. 27(3):185-91, 1983
Type of study:
randomized controlled clinical trial
Control/comparison:
attention and conventional medical care
Sample characteristics:
30 patients matched on age, sex, pre-treatment and acne severity
Type of intervention:
biofeedback-assisted relaxation and cognitive imagery treatment, 12 sessions over six weeks
Primary outcome measure(s):
acne severity as measured by Cook, Centner and Michaels photographic standards
Outcome:
The treatment resulted in a significant reduction of acne severity compared to the attention and medical care. Treatment group patients who continued home practice until follow-up maintained their gains, whereas those who discontinued failed to maintain gains.
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Herbal Medicine
Author(s):
Bassett IB, Pannowitz DL, Barnetson RS
Institution:
Department of Dermatology, Royal Prince Alfred Hospital, Camperdown, NSW
Title:
A comparative study of tea-tree oil versus benzoylperoxide in the treatment of acne
Source:
Medical Journal of Australia. 153(8):455-8, 1990
Type of study:
randomized controlled clinical trial.
Control/comparison:
efficacy and skin tolerance of 5% benzoyl peroxide
Sample characteristics:
124 patients with mild to moderate acne
Type of intervention:
use of 5 tea-tree oil gel on skin
Primary outcome measure(s):
number of inflamed and non-inflamed lesions (open and closed comedones)
Outcome:
The results of this study showed that both 5% tea-tree oil and 5% benzoyl peroxide had significant effect in ameliorating the patients’ acne by reducing the number of inflamed and non-inflamed lesions (open and closed comedones). Although the onset of action in the case of the tea-tree oil was slower, fewer side effects were experienced by the patients treated with tea-tree oil.
Author(s):
Higaki S., Nakamura M., Morohashi M, et al.
Institution:
Dr. S. Higaki, Department of Dermatology, Faculty of Medicine, Toyama Medical/Pharmaceutical University , 2630 Sugitani, Toyama-she 930-01, Japan
Title:
Activity of eleven Kampo formulations and eight Kampo crude drugs against Propionibacterium acnes isolated from acne patients: Retrospective evaluation in 1990 and 1995
Source:
Journal of Dermatology. 23: 871-875, 1996
Type of study:
in vitro lab study
Control/comparison:
comparing the minimum inhibitory concentrations (MIC) in 1990 and 1995 of 11 Kampo formulations and 8 Kampo crude drugs against Probionibacterium acnes isolated from acne
Sample characteristics:
Propionibacterium acne strains
Type of intervention:
11 Kampo formulations and 8 Kampo crude drugs
Primary outcome measure(s):
Primary outcome measure(s): examining the minimum inhibitory concentrations (MIC) in 1990 and 1995 of 11 Kampo formulations and 8 Kampo crude drugs against Probionibacterium acnes isolated from acne
Outcome:
Probionibacterium acne strains were most sensitive to Oren-gedoku-to (OGT) among these Kampo formulations. Coptidis Rhizoma (CR) and Phellodendri Cortex (PC) inhibited the growth of Probionibacterium acnes significantly among the eight Kampo crude drugs examined. No significant increases in MIC of Kampo formulations and Kampo crude drugs to Probionibacterium acne were observed. The speculation was made that Kampo crude drugs such as CR and PC were better than minocycline or erythromycin from the point of a progressive increase in MIC to Probionibacterium acne. CR and PC, which were each an ingredient of OGT, might contain some components with strong antibacterial activity to Probionibacterium acne.
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Nutrition/Supplementation
Author(s):
Vahlquist A, Michaelsson G, Juhlin L
Institution:
Department of Dermatology, University Hospital, Uppsala, Sweden
Title:
Acne treatment with oral zinc and vitamin A: effects on the serum levels of zinc and retinol binding protein (RBP)
Source:
Acta Dermato-Venereologica. 59(5):437-42, 1978
Type of study:
randomized controlled clinical trial
Control/comparison:
vitamin A and placebo
Sample characteristics:
75 patients with acne, 53 males and 22 females, between the ages of 15 and 25 years old
Type of intervention:
oral treatment with zinc sulphate effervescent tablets
Primary outcome measure(s):
serum zinc level after 2 and 4 weeks and 3 months, clinical improvement of acne
Outcome:
There was an increase in the mean serum zinc level in the zinc-treated patients after 2 weeks, the time when the first clinical improvement occurred. After 4 weeks the zinc level had increased by about 30% and no further significant increase was observed during 3 months of treatment. In the 33 healthy subjects there was an increase of 14% after 4 weeks of zinc therapy. Vitamin A and placebo induced no significant changes in the serum zinc status.
Author(s):
Vahlquist A, Michaelsson G, Juhlin L
Institution:
Department of Dermatology and Clinical Research, Uppsala University Hospital, Uppsala, Sweden
Title:
Effects of oral zinc and vitamin A in acne
Source:
Archives of Dermatology. 113(1):31-6, 1977
Type of study:
controlled clinical trial
Control/comparison:
vitamin A and placebo
Sample characteristics:
64 patients, 38 male and 26 female, between 13 and 25 years of age with grades 2 to 4 acne.
Type of intervention:
135 mg oral zinc sulfate daily alone and in combination with 300,000 IU vitamin A daily on acne lesions
Primary outcome measure(s):
change in number of comedones, papules, pustules, and infiltrates were counted at each visit
Outcome:
After 4 weeks there was a significant decrease in the number of papules, pustules, and infiltrates in the zinc-treated groups. The effects of zinc plus vitamin A was not better than zinc alone. After 12 weeks of treatment, the mean acne score had decreased from 100% to 15%. The mechanism for the effect of zinc therapy in acne is not presently known.
Author(s):
Gandola M, Argeniano G, Barba C, et al.
Institution:
Title:
Topical vitamin A acid in the treatment of acne vulgaris (a controlled multicenter trial)
Source:
Archives of Dermatological Research - Archiv fur Dermatologische Forschung. 255(2):129-38, 1976
Type of study:
controlled multi-center trial
Control/comparison:
salicylic acid and placebo
Sample characteristics:
211 acne patients in comparable groups
Type of intervention:
application of topical retinoid acid against sulfur-resorcinol--salicylic acid and placebo
Primary outcome measure(s):
uniform evaluation criteria
Outcome:
After 8 weeks' treatment in comparable groups of patients, retinoic acid proved to be superior to the standard and to the placebo. The difference was statistically significant. Side effects were present in a number of patients treated with the active substances and with the placebo (mainly erythema), but rarely was the treatment discontinued.
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