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临床试验/CTRI/2014/07/004796
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

VIdya Herbs0 个研究点目标入组 30 人开始时间: 待定最近更新:

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

发起方
VIdya Herbs

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