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Clinical study on Anti-acne spot oil in pimples

Phase 2
Completed
Conditions
Health Condition 1: L700- Acne vulgaris
Registration Number
CTRI/2022/07/044013
Lead Sponsor
amaskar Ayurved Private Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
30
Inclusion Criteria

1.Subjects suffering from acne vulgaris [mild and moderate as per Global Acne Grading System (GAGS)] as diagnosed by physician or dermatologist

2.Subjects willing to follow study instructions given by the investigator

Exclusion Criteria

1.Subjects with known pre-existing systemic disease necessitating long-term medications.

2.Subjects with known current endocrinal disorders.

3.Subjects taking treatment for menstrual disorders

4.Subjects having systemic treatment for acne vulgaris.

5.Subjects on any other investigational products within 1 month prior to randomization;

6.Subjects with known current tuberculosis, HIV, ischemic heart disease, cancer, kidney failure.

7.Pregnant and lactating women

8.Known hypersensitivity to any of the ingredients of Anti-acne Spot Oil

9.Other conditions, which in the opinion of the investigators, make patient unsuitable for enrolment or could interfere with his/her participation in, and completion of the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in total number of inflammatory acne lesions on faceTimepoint: Screening / Baseline visit (Day 0), Visit 1 (24 hrs. post skin patch test application), Visit 2 (48 hrs. post skin patch test application) visit 3 (Day 15), visit 4 (Day 30)
Secondary Outcome Measures
NameTimeMethod
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