Table 1.
Author | Sample size | Age | Sex | Study design | Disease category | Diagnostic and evaluating criteria | Treating method | Treating duration | Dropout | Major outcome parameter | Side effect | ||
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Treatment group | Control group | Treatment group | Control group | ||||||||||
Sheehan and Atherton 1992 | 47 | 1.5–18.1 years | Male: 27 Female: 20 |
Placebo-controlled, double-blind, crossover trial | Nonexudative atopic eczema | Simple scoring system | Traditional Chinese herbal formula (PSE101) versus placebo | 5 months (assessed at 4 weekly intervals) | 10 | (1) Median clinical score for erythema and surface damage. (2) Clinical scores change for treatment group and control group. (3) The percentage changes of median and 95% CI median of clinical scores. |
Eosinophilia and elevated serum IgE levels. | ||
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Fung et al. 1999 | 40 | 7–50 years |
Male: 19 Female: 18 |
Double-blind, placebo-controlled, crossover study | Recalcitrant atopic dermatitis | The severity and extent of four clinical parameters (erythema, surface damage, lichenification, and scaling) | Traditional Chinese herbal formula (Zemaphyte) versus placebo | 20 weeks (assessed at 4 weekly intervals) | 3 | (1) The median clinical scores variation for erythema, surface damage, lichenification, and scaling. (2) The comparison of median clinical scores at fourth week between the treatment group and control group. (3) The personal tendency of patients for Zemaphyte and placebo. (4) Complete blood picture and renal and liver function tests. |
Hair loss, transient dizziness, gastrointestinal upsets, lichenoid eruption. | ||
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Lun and Rong 2000 | 25 | 25 | 15–60 years | Male: 31 Female: 19 |
Randomized controlled trial | Intractable cutaneous pruritus | — | Auricular acupuncture versus combination of cyproheptadine and calamine lotion | 5 weeks | 0 | Therapeutic effects between two groups (curing, markedly effective, effective, ineffective). | No report. | |
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Bai et al. 2007 | 120 | 15–60 years (mean age: 27.45 years) | Male: 42 Female: 78 |
Randomized controlled trial | Acute eczema | Clinical criteria of acute eczema comes from Clinical Dermatology | Traditional Chinese medicine method (Shuangfujin) versus normal saline group; boric acid group; Pikangwang group | 4 days | 0 | (1) Clinical score variation of skin damage. (2) Clinical score variation of pruritus. (3) The total clinical effectiveness and basic recovery comparison. (4) Adverse effects. (5) Syndrome improvement. (6) Laboratory index. |
Regional erythema eruption and burning sensation. | ||
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Hon et al. 2007 | 42 | 43 | 5–21 years | Male: 23 Female: 19 |
Male: 23 Female: 20 |
Randomized, double-blind, placebo-controlled study | Atopic dermatitis | SCORAD; CDLQI; allergic rhinitis score |
Traditional Chinese herbal medicine concoction versus placebo | 12 weeks | 0 | (1) Improvement from baseline in mean SCORAD. (2) Improvement from baseline in mean CDLQI scores. (3) Blood counts, eosinophil counts, total IgE levels, and liver and renal function. |
Upper respiratory tract; infection; diarrhoea; abdominal pain; episodes of asthma. |
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Chen et al. 2008 | 38 | 37 | 18–54 years | Male: 3 Female: 35 |
Male: 5 Female: 32 |
Randomized controlled trial | Facial corticosteroid addictive dermatitis | Clinical criteria for facial corticosteroid addictive dermatitis and TCM syndrome differentiation criteria (Xuexufengzao) | Modified Wuhua decoction combined with levocetirizine versus levocetirizine | 30 days | 12 | (1) Clinical scores. (2) The variation of symptom score before and after treatment. (3) The variation of skin erythema and TEWL before and after treatment. (4) Adverse effect. |
Gastrointestinal upsets; mild drowsiness. |
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Senapati et al. 2008 | 25 | 25 | Treatment group mean age: 16.09 years; control group mean age: 17.46 years |
Male: 11 Female: 14 |
Male: 7 Female: 18 |
Randomized placebo-controlled trial | Atopic dermatitis | Hanifin and Rajka criteria: diagnostic features of atopic dermatitis; IISA | Evening primrose oil versus placebo | 5 months | 12 | (1) The scores of study cases at baseline and at five monthly evaluations. (2) Effect of evening primrose oil versus placebo on total scores of patients of atopic dermatitis. (3) Adverse effect. |
Not found. |
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Shi et al. 2008 | 25 | 22 | Treatment group: 14–32 years; control group: 15–31 years |
Male: 14 Female: 11 |
Male: 12 Female: 10 |
Randomized controlled trial | Atopic dermatitis | The UK working party's diagnostic criteria for atopic dermatitis derivation | Jiaweidangguiyin combined with loratadine versus loratadine | 4 months | 0 | (1) The clinical effectiveness comparison between experimental group and control group. (2) The cytokine levels comparison before and after treating. (3) Safety and adverse effect. |
Not found. |
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Xu et al. 2008 | 22 | 20 | Treatment group: 52.09 ± 16.94 years; control group: 43 ± 16.53 years |
Male: 10 Female: 12 |
Male: 10 Female: 10 |
Randomized controlled trial | Chronic eczema | Clinical criteria of chronic eczema comes from Clinical Dermatology and TCM syndrome differentiation criteria (Xuexufengzao); SSRI and Eczema Area and Severity Index score | Herbal Saxifrage cream versus hydrocortisone | 4 weeks | 0 | (1) Symptom score before treatment and SSRI after treatment in two groups. (2) Clinical efficacy in two groups. |
No report. |
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Gao et al. 2009 | 30 | 30 | Treatment group: 35.6 ± 13.8 years; control group: 37.5 ± 12.9 years |
Male: 13 Female: 17 |
Male: 11 Female: 19 |
Randomized controlled trial | Chronic urticaria | Chronic urticaria comes from the TCM disease diagnostic and effective criteria | Penetrative needling of Shendao versus levocetirizine hydrochloride | 12 weeks | 0 | (1) Comparison between acupuncture and medication groups in the symptom scores. (2) Comparison between acupuncture and medication groups in serum IgE level. |
No report. |
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Kobayashi et al. 2010 | 37 | 40 | 20–40 years | — | A 6-month, Multicenter, double-blind, randomized, placebo-controlled study |
Atopic dermatitis | The scoring system by the Atopic Dermatitis Severity Evaluation Committee of Japanese Dermatological Association |
Traditional herbal medicine (Hochu-ekki-to) versus placebo | 24 weeks | 14 | (1) Clinical efficacy of Hochu-ekki-to(time course change of skin severity score during examination; time course change of equivalent dosage of topical agent during examination). (2) Adverse effects and abnormal laboratory findings. |
No report. | |
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Pfab et al. 2010 | 30 | 18–50 years | Male: 16 Female: 14 |
A blinded, randomized, placebo-controlled, crossover trial |
Atopic dermatitis | Visual analogue scale and the Eppendorf Itch Questionnaire | Acupuncture versus placebo | 10 minutes | 0 | (1) Wheal and flare size. (2) Skin perfusion measured at the stimulus site. (3) The validated Eppendorf Itch Questionnaire. |
No report. | ||
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Cheng et al. 2011 | 47 | 24 | Treatment group mean age: 12.2 years; control group mean age: 13.6 years | Male: 25 Female: 22 | Male: 12 Female: 12 | A randomized, double-blind, placebo-controlled trial |
Refractory atopic dermatitis | Hanifin and Rajka criteria: diagnostic features of atopic dermatitis |
Chinese herbal product (Xiao-Feng-San) versus placebo | 8 weeks | 10 | (1) Improvement in scores (clinical lesion; erythema; surface damage; pruritus; sleep) between baseline and week 8. (2) Score improvement (clinical lesion; erythema; surface damage; pruritus; sleep) from baseline to weeks 4, 8, and 12. (3) Immunologic markers variation before and after treatment. (4) Laboratory index. |
Transient elevation of aspartate aminotransferase; gastrointestinal upsets. |
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Hon et al. 2012 | 42 | 43 | 5–21 years | — | Randomized, double-blind, placebo-controlled study | Atopic dermatitis | Hanifin and Rajka criteria: diagnostic features of atopic dermatitis; SCORAD; allergic rhinitis scores; the Children's Dermatology Life Quality Index |
Traditional Chinese herbal medicine versus placebo | 12 weeks | 0 | (1) Percentage improvement of SCORAD from baseline. (2) The total allergic rhinitis scores between two groups. (3) Adverse effects. |
Not found. | |
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Pfab et al. 2011 | 5 | 5 | Mean age: 25.2 ± 4.5 | Male: 8; female: 2 | Unicenter, single-blinded, prospective, randomized clinical pilot trial |
Atopic eczema | Visual analogue scale; SCORAD | Acupuncture versus blank group | 33 days | 0 | (1) SCORAD comparison between two groups. (2) Itch intensity (VAS) between two groups. (3) Basophil activation test comparison between two groups. |
No report. | |
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Xiu and Wang 2011 | 100 | 100 | Treatment group: 14 months to 60 years; control group: 2 to 65 years | Male: 60 Female: 40 | Male: 55 Female: 45 |
Randomized controlled trial | Chronic urticaria | — | Acupoint injection with autoblood versus medicine group | 30 days | 0 | (1) Clinical effectiveness comparison between two groups. (2) The mean onset time between two groups. (3) The cured numbers for different kinds of chronic urticaria. |
No report. |
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Choi et al. 2012 | 12 | 12 | Treatment group: 18.6 ± 8.4 years; control group: 14.2 ± 6.0 years old | Male: 5 Female: 7 | Male: 5 Female: 7 | Parallel, randomized, active-controlled, double-blind trial | Atopic dermatitis | Hanifin and Rajka criteria: diagnostic features of atopic dermatitis and dampness-heat pattern type of AD; SCORAD and EASI score | TJ-15 combined with TJ-17 versus TJ-15 | 4 weeks | 5 | (1) Change of SCORAD score. (2) Change of EASI score. (3) Clinical safety evaluated by laboratory index. |
No report. |
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Lee et al. 2012 | 8 | 7 | 19–79 years; treatment group median age: 34 years; control group median age: 36 years | Male: 4 Female: 4 |
Male: 6 Female: 1 | Single-center, randomized controlled trial | Atopic dermatitis | VAS scores, EASI scores, and IGA | Acupressure versus using any prescription or over-the-counter medications or lotions (except acupressure technique) | 4 weeks | 0 | (1) Change in VAS between control and experimental groups. (2) Change in IGA score between control and experimental groups. (3) Change in EASI score between control and experimental groups. |
No report. |
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Pfab et al. 2012 | 20 | Mean age: 23.3 ± 1.7 years | Male: 6 Female: 14 |
A patient- and examiner-blinded, randomized, placebo-controlled, crossover trial |
Atopic dermatitis | Atopic dermatitis diagnosis [scoring atopic dermatitis (SCORAD) > 20]; VAS; EIQ | VAp, VAa, VC versus PAp, PAa, and PC | 20 minutes | 0 | (1) Mean itch intensity. (2) Wheal and flare size. (3) Qualitative assessment of itch intensity (EIQ). (4) Mean attention scores. (5) Evaluation of blinding. |
No report. | ||
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Wu et al. 2012 | 50 | 35 | 18–70 years | Male: 28 Female: 22 | Male: 15 Female: 20 | Randomized controlled trial | Atopic dermatitis | Clinical criteria of chronic urticaria comes from Clinical Dermatology | Yiqi Huoxue Qufeng decoction versus Fuyang granule | 8 weeks | 0 | (1) The clinical effects comparison between two groups. (2) The DAO comparison between two groups. (3) The positive rate of IgE comparison between two groups. |
No report. |
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Quan et al. 2014 | 30 | 30 | Treatment group: 24.3 years; control group: 23.45 years |
Male: 13 Female: 16 |
Male: 14 Female: 16 | Randomized controlled trial | Atopic dermatitis | The western medicine diagnostic criteria and traditional Chinese medicine diagnosis standard; SCORAD scores | Flying needle combined with herbal medicine versus herbal medicine combined with regular skin-care | 3 months | 1 | (1) The comparison of SCORAD scores. (2) Total effective rate. (3) Side effect. |
No report. |
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Liu et al. 2015 | 250 | 5–25 years | Male: 107 Female: 143 |
Randomized controlled trial | Atopic dermatitis | The criteria of Hanifin and Rajka; SCORAD; QoL scores; self-assessment scores | PTQXT versus combination TCM therapy versus control group (mometasone furoate) | 12 weeks | 0 | (1) Efficacy outcomes (SCORAD, QoL scores, self-assessment scores). (2) Adverse effects. (3) Test of blinding. |
Slight diarrhoea. | ||
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Mehrbani et al. 2015 | 24 | 18 | Treatment group: 28.62 ± 2.30 years; control group: 24.33 ± 1.50 years | Male: 4 Female: 20 | Male: 2 Female: 16 | A randomized, double-blind, placebo-controlled clinical trial |
Moderate-to-severe atopic dermatitis | The criteria of Hanifin and Rajka | Dodder seed extract versus placebo | 15 days | 10 | (1) Efficacy. (2) Safety profile. |
Anorexia; mild gastrointestinal problems. |
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Yen and Hsieh 2016 | 16 | 17 | Treatment group: 32.9 ± 13.4 years; control group: 39.6 ± 12.3 years | Male: 10 Female: 5 | Male: 10 Female: 6 | A preliminary, randomized, controlled, open-label study | Atopic dermatitis/ eczema | The criteria of Hanifin and Rajka; EASI scores and TIS scores | TYO (Tzu-Yun ointment) versus TS cream (topical steroid) | 8 weeks | 0 | (1) Effect of TYO and TS cream on EASI and TIS scores in patients with eczema/atopic dermatitis. (2) Comparison between effects of TYO and TS cream on EASI and TIS scores in patients with eczema/atopic dermatitis. |
No report. |
Note. SCORAD: SCORing Atopic Dermatitis; CDLQI: Children's Dermatology Life Quality Index; IISA: Intensity Item Score Aggregate; TCM: traditional Chinese medicine; SSRI: Symptom Score Reducing Index; EASI: Eczema Area and Severity Index; VAS: visual analogue scale; IGA: Investigator's Global Assessment; EIQ: Eppendorf Itch Questionnaire; QoL: Quality of Life; PTQXT: Pei Tu Qing Xin Tang; TIS: Three-Item Severity.