MedPath

A study to assess how effective and safe is the moisturizer for patients having acne who areprescribed isotretinoi

Phase 4
Completed
Conditions
Health Condition 1: L988- Other specified disorders of the skin and subcutaneous tissue
Registration Number
CTRI/2019/07/020458
Lead Sponsor
Cipla Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
200
Inclusion Criteria

1. A voluntarily given, written signed dated data sharing consent from participants and/or legally acceptable representative.

2. Participants of 18 years and above of either gender who are newly prescribed Isotretinoin or who have not used oral isotretinoin for past one month for the management of acne and moisturiser (Excela) as an adjuvant therapy as per Investigatorââ?¬•s discretion.

Exclusion Criteria

1.Any skin allergy or serious skin condition or unsuitable to participate in the study as per routine clinical practice.

2.Pregnant and lactating women

3.Participated in any clinical trial within 1 month from screening

Study & Design

Study Type
PMS
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath