CTRI/2014/07/004796已完成未知
A Prospective, Randomized, Double blind, Placebo controlled clinical trial to evaluate efficacy and safety of MUKUL PURE in treating Acne
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- VIdya Herbs
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Both Male / Female of age between 18-50 yrs
- •Facial acne, with:
- •1.Inflammatory facial lesions (papules/pustules/nodules/cysts)
- •2.Non inflammatory facial lesions if open (blackhead) and if closed (whitehead) comedones
- •3.Mild to moderate acne with nodular abcesses, extensive lesions
- •Willing to give written informed consent along with audio, video recording
排除标准
- •Patient not willing to comply with the study procedure
- •Females who are pregnant or breast-feeding
- •Skin diseases other than acne vulgaris
- •Use of other topical or systemic treatments for acne
- •Other significant medical conditions or clinically significant abnormal laboratory test results
- •History of alcoholism or substance abuse and any other liver abnormalities
- •Conditions in the opinion of the investigator make the patient unsuitable to participate in the study.
- •History of Hormone-sensitive condition such as breast cancer, uterine cancer, ovarian cancer, endometriosis, or uterine fibroids
- •Patients under medication with contraceptive pills, Diltiazem, Anticoagulant and Propranolol.
- •History of hypothyroidism or hyperthyroidism
- •History of HIV
- •Participation in another trial within 3 months prior to informed consent
- •Certain medications that may interfere with the study medication (these will be identified by the study doctor).
研究者
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