| Sebum Production Studies |
| Green tea | GT formulation: 5% green tea; GT-L formulation: 2.5% green tea + 2.5% lotus extract. | Green tea (GT) Topical | Green tea + Lotus (GT-L) Topical; Placebo Topical | n = 22; all healthy men; Age 22–28 years-old. | Single-blinded, placebo-controlled, monocentric study; Pakistan (months December-February); 2 groups (G): G1: used GT topical on one cheek, placebo on the other; n = 11;G2: GT-L topical on one cheek, placebo on the other; n = 11. Intervention length: 60 days; Amount of tea polyphenol: information not provided; Frequency of application: once daily at bedtime; Follow up time: baseline, day 15, 30, 45, 60; Sebum excretion on both cheeks measured with Sebumeter at each visit. | Percent change in sebum secretion every 15 days (calculated by formula % change = ((Dx − D0)/D0) × 100; Dx = sebum value on day 15, 30 45, 60; D0 = baseline sebum value) | G1 (GT group): significant reduction in sebum secretion from baseline to 60 days of treatment compared to placebo control (p = 0.0060) (27% decrease from baseline); G2 (GT-L group): significant reduction in sebum secretion from baseline to 60 days of treatment compared to placebo control (p = 0.0002) (25% decrease from baseline); Placebo: no significant effect on reducing sebum secretion. | None reported | Mahmood et al., 2013 [15] |
| Green tea | 3% GT extract | Topical | No control group | n = 10; Age 24 to 40 years-old; all healthy men | Therapeutic studyIntervention length: 60 days;Frequency of topical use: not stated;Amount of topical: not stated;Follow up: skin sebum production measured at week 1, 2, 3, 4, 6, and 8 via sebumeter. | Percent change in skin sebum production (calculated via formula % change = ((A − B)/B) × 100A = individual value of any parameter (from 1st to 8th week);B = zero value for that parameter. | 3% GTE formulation decreased sebum production by nearly 10% at week 1, and 60% at week 8) (p < 0.05) |
| Mahmood et al., 2010 [34] |
| Acne Studies |
| Green tea | Amount of tea polyphenols: Each GTE capsule contained:285.6 mg EGCG,78.7 mg ECG,38.5 mg EGC,24 mg EC,21.25 mg GCG,<0.3 mg GC,<0.3 mg caffeine,51.65 mg cellulose | SystemicDecaffeinated GTE; each capsule 500 mg decaffeinated GTE or cellulose | Placebo (cellulose) | n = 80;All women;Age 25–45 years-old with moderate to severe acne (determined by Investigator’s Global Assessment (score of 3 or 4 on a scale 0 to 5));None of the women received systemic retinoid or hormone treatment during previous 3 months. | Randomized, double blind, placebo controlled trial;May 2012 to October 2013, Taiwan;Intervention length: 4 weeks;Follow up: baseline and at 4 weeks;G1: received decaffeinated GTE for 4 weeks n = 40;G2: placebo (pure cellulose) for 4 weeks n = 40;Products packaged into identical capsules for blinding purposes;Frequency: Subjects took 1 capsule 30 min after meals 3 times daily for 4 weeks. | Acne lesion counts (inflammatory and non-inflammatory) recorded for entire face by blinded dermatologist at baseline and at 4 weeks | Between group comparison: G1 vs. G2: significant reduction in inflammatory lesion counts on nose (p = 0.03), perioral area (p = 0.04) and chin (p = 0.03); no difference in total lesion count;G1 did not have significant reduction on forehead, cheek and total lesion count compared to placebo;Within group comparison:G1: Compared with baseline, G1 (decaffeinated GTE) had significantly lower number of inflammatory lesions on forehead (p = 0.04), cheeks (p = 0.04) and entire face (total lesion count) (p = 0.003); G2: in placebo group, there was significant reduction in inflammatory lesion count on cheeks (p = 0.01), chin (p = 0.01) and entire face (p = 0.02). | G1: 1 subject developed mild constipation, 2 subjects abdominal discomfort after GTE treatment; G2: 1 subject thirsty, 1 difficulty falling asleep; No major adverse effects noted. | Lu et al., 2016 [39] |
| Tea | Apple brand tea leaves; Amount of tea polyphenol: not stated | Topical2% tea lotion; | 5% zinc sulphate solution | n = 47; 33 females; 14 males; Age 13–27 years-old with acne vulgaris (severe acne excluded); Excluded comedonal, severe acne and nodulo-cystic acne and if on acne treatment in past 2 months; also systemic disease therapy with ie corticosteroids, hormones, medications that induce acniform rash. | Single-blind randomly comparative therapeutic clinical trial; Iraq, June 2006 to December 2007; Intervention length 8 weeks; Frequency of topical: twice daily; G1: 2% tea lotion n = 24 (17 females, 7 males); G2: 5% zinc sulphate solution n = 23 (16 females, 7 males); Follow up: Inflammatory (papules and pustules) lesions counted every 2 weeks for a total of 8 weeks; Photograph taken at baseline and subsequent visits. | Clinical improvement of acne vulgaris—scored by inflammatory lesion counting before and after treatment:Mild acne: <20 pustules and <10 papules;Moderate acne: 20–40 pustules, >30 papules).Good response: inflammatory (papules and pustules) lesion count decrease by >50%; Moderate response: lesion count decrease between 10% and 50%; No response: reduction in lesion count <10%. | n = 40 completed the study; n = 20 in each group;G1: 2% tea lotion statistically significant decrease in number of inflammatory lesions;Response to treatment:15%—no response;25%—moderate;60%—good. Papule count before treatment 23.3 ± 10.9; After treatment 12 ± 8.7, statistically significant difference (p = 0.0001).Pustule count before treatment 29.5 ± 5.8;After treatment 14.5 ± 10.7, statistically significant reduction (p < 0.001).G2: zinc sulphate beneficial but result not statistically significantResponse to treatment:35%—no response;50%—moderate;15%—good.Papules before treatment 19.5 ± 9.7 and after treatment 14.4 ± 8.6 (reduction not statistically significant; p = 0.08);Pustules before treatment 19.4 ± 9.3 and after treatment 15.2 ± 9.5 (reduction not significant; p = 0.16). | G1: 5 subjects (25%): mild itching only in early course of treatment which then disappeared;G2: burning sensation in 5 subjects (25%), itching in 2 (10%) in early course of treatment which was subsequently reduced;No major adverse effects. | Sharquie et al., 2008 [35] |
| Green tea | EGCG | 1% EGCG and 5% EGCGTopical | Vehicle with 3% ethanol | n = 35;17 men;18 women;mean age: 22.1 (range not stated). | Randomly assigned split body trial;Intervention length: 8 weeks;Follow up: baseline, week 1, 2, 4, 6, and 8;Frequency of application: twice daily;Amount per application: not stated;G1: used 1% EGCG, n = 17;G2: used 5% EGCG, n = 18;Both groups applied lotion to one side of face, vehicle containing 3% ethanol to the other. | Dose response relationship between 1% and 5% EGCG in improving acne lesion count;Leeds grading and acne lesion count to calculate changes in non inflammatory lesions (whiteheads, blackheads, comedones) and inflammatory lesions (papules, pustules, nodules) during EGCG application period. | Baseline Leeds score: 5.1 ± 0.4;Week 8 Leeds score:1.2 ± 0.4 (1% EGCG); 1.7 ± 0.6 (5% EGCG); 1% EGCG resulted in:79% reduction of non-inflammatory acne (53.8 ± 19.8 mean lesions at baseline, 15.6 ± 6.2 at week 8, p < 0.05);89% reduction in inflammatory acne (10 ± 3.1 mean lesions at baseline, 1.1±0.5 at week 8, p < 0.05); 5% EGCG significantly improved inflammatory and non-inflammatory lesion counts (p < 0.05), but details not provided. |
| Yoon et al., 2013 [31] |
| Tea | Swan brand tea | Topical2% tea lotion: (prepared by adding 75 mL tea extract + 25 mL ethanol (95% purity)) | Control lotion: (prepared by adding 75 mL distilled water + 25 mL ethanol (95% purity)) | n = 60;25 males;35 females;Age 14–22 years-old. | Iraq, October 2002 to October 2004;Intervention length: 2 months;Follow up: at 1 and 2 months;Frequency of topical application: twice daily;Amount applied: not stated;2 groups: G1: n = 30, mean age 17.5 ± 3.9 years, treated with 2% tea lotion twice per day for 2 months, clinical evaluation monthly (inflammatory lesion count—papules and pustules).G2: n = 30, mean age 18.1 ± 3.7 years treated in the same manner but with control lotion. | Inflammatory lesion count (papules and pustules) assessed as follows: Mild acne: < 20 pustules, papules < 10;Moderate acne: 20–40 pustules, 10–30 papules; Severe acne: pustules > 40, papules > 30.Response to treatment classified as: Good response: >50% reduction in inflammatory lesion count; Moderate response: 10%–50% reduction in inflammatory lesion count; No response: <10% reduction in inflammatory lesion count. Patient satisfaction to treatment assessed as:- full satisfaction- partial satisfaction- no satisfaction | n = 49 completed treatment;G1: n = 25 Significant reduction in lesion count of papules (baseline 12 ± 3.3, week eight 8.1 ± 0.19, p < 0.001) and pustules (baseline 20.7 ±5.8, week eight 8.9 ± 2.3, p < 0.001);G2: n = 24. No significant reduction of papules or pustules at 8 weeks compared to baseline.Patient satisfaction after 8 weeks:G1: 64% fully satisfied, 6 patients (24%) partially satisfied, 12% not satisfied;G2: 83.3% not satisfied, 12.5% partially satisfied, 4.2% fully satisfied. | None | Sharquie et al., 2006 [36] |
| Green tea |
| Topical2% green tea lotion (prepared by adding 75 mL tea extract + 25 mL ethanol (95% purity) |
| n = 20;6 males;14 females;Age 15–36 years old. | Egypt, May 2007 to February 2008;Intervention length: 6 weeks;Follow up: every 2 weeks;Frequency of application: twice daily;Amount of topical applied: not stated;Acne severity assessed, baseline photographs taken, green tea lotion given to be applied on face twice daily for 6 weeks, follow up every 2 weeks;TLC considered 100% at baseline and any decrease was considered improvement. | Change in TLC and SI scores at the end of treatment compared to baseline;Acne severity assessed every 2 weeks via total lesion count (TLC) and severity index (SI);TLC = papules + pustules;SI was determined as follows: SI = 1 if TLC < 10SI = 2 if TLC = 10–20SI = 3 if TLC > 20 | Mean TLC decreased from 24 (baseline) to 10 after 6 weeks of treatment (58.33% reduction, p < 0.0001, 95% CI = 8.58–19.42);Mean SI decreased from 2.05 (baseline) to 1.25 after 6 weeks of treatment (39.02% reduction, p < 0.0001, 95% CI = 0.54–1.26). | Stinging sensation in 2 subjects (10%) on first day of lotion use, disappeared in 48 h;Minimal pruritus in 3 of 20 subjects (15%) on first day of lotion use and lasted 3 days. | Elsaie et al., 2009 [37] |
| Green tea | Polyphenon-60 (green tea extract compound) | Topical20 mg/mL polyphenon-60 applied to face twice daily for 8 weeks | None | n = 30,with mild to moderate acne;Age: not stated;Proportion of sex: not stated. | Therapeutic study;Intervention length: 8 weeks;Follow up time: baseline and at 8 weeks;Frequency of application: twice daily;Amount applied: not stated;KoreaTopical polyphenon-60 (20 mg/mL) from green tea lotion applied onto facial acne twice daily for 8 weeks;Acne lesion count at baseline and at 8 weeks done by dermatologists. | Acne lesion count: open comedones, closed comedones, and pustules at baseline vs. 8 weeks after treatment | 8 weeks post-treatment compared to baseline: Number of open comedones decreased by 61% (p < 0.05);Number of pustules decreased by 28% (p < 0.05);Number of closed comedones was not significantly decreased. |
| Jung et al., 2012 [38] |