CTRI/2024/01/061604已完成Unknown
A Single Center, Randomized, Interventional, Active Controlled, Parallel Group Study To Evaluate The Efficacy And Safety Of Lactoferrin Containing Cream In The Treatment Of Patients With Mild To Moderate Acne Vulgaris. - Nil
Frimline Private Limited0 个研究点目标入组 80 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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
- •1. Male and Female patients with age 18 - 65 years, with acne vulgaris of face.
- •2. Written informed consent signed by patient and willing to comply with the study procedure.
- •3. Patients with mild to moderate acne, as determined by an Investigator Global Assessment (IGA) score of 2 to 3.
- •4. Females of childbearing potential must have a negative pregnancy test at screening and agree to use an acceptable form of contraception during the study.
排除标准
- •1. Pregnant Lactating females.
- •2. Previous hypersensitivity or allergic reaction to any of the components in the study medication.
- •3. Patients with the skin conditions of the face such as open or incompletely healed wounds at the affected site or acute eczemas, rosacea, perioral dermatitis, atopic-seborrheic dermatitis or psoriasis.
- •4. Use of topical acne medication within the past 1 weeks.
- •5. Any significant dermatological condition or skin infection other than acne vulgaris that may interfere with the study assessments.
- •6. Patients with the significant cardiovascular, hepatic, renal or any other systemic illnesses.
- •7. Use of any Investigational drug or participation in another clinical trial within the past 30 days.
- •8. Any other medical or psychological condition that, in the opinion of the investigator, may interfere with the patients ability to participate in the study or complete the study assessments.
- •9. Any condition or situation that, in the investigators judgment, may put patient at risk or compromise the integrity of the study.
研究者
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