primary irritation patch test on healthy human volunteers

Completed

Brief Summary: Study Objective:The objective of this study is to evaluate thedermatological safety of the investigational products on healthy humansubjects.

Study Population: 24 healthy human volunteers (Male and Female1:1) with Skin types (Oily, Dry, Normal and Combination, 1:1:1:1 ratio).

Duration of study: Approximately 9 days for eachvolunteer.

Test Site: Between the scapula and waist of thesubjects, the test site should be free of pigmentation, pimple, hair, mole orany dermatological condition that can interfere with the reading.

This patch will then beapplied on the test site. The patch will be kept for 24 hours. After which thepatches will be removed and the first observation will be made at 30 minutes ofpatch removal (0 hr. observation). The further observations will be at 24 hrsand 1 week of patch removal

Recruitment & Eligibility

Inclusion Criteria

1.Subjects in age group 18.
55 years (both the ages inclusive). 2.Healthy male & female subjects. 3.Subjects with Fitzpatrick skin type III to V. 4.Subjects willing to give a voluntary written informed consent. 5.Subjects willing to maintain the patch test in position for 24 hours. 6.Subject having not participated in a similar investigation in the past two weeks. 7.Subjects willing to come for regular follow up visits. 8.Subjects ready to follow instructions during the study period.

Exclusion Criteria

1.Infection, allergy on the tested area.
2.Skin allergy, antecedents or atopic subjects.
3.Athletes and subjects with history of excessive sweating.
4.Cutaneous disease which may influence the study result.
5.Subjects on oral corticosteroid.
6.Subjects participating in any other cosmetic or therapeutic trial.
7.Any history of underlying uncontrolled medical illness including diabetes, liver disease or history of alcoholism, HIV or any other serious medical illness.

Primary Outcome Measures

Name	Time	Method
To evaluate the dermatological safety of the investigational products	Approximately 9 days for each volunteer.

Secondary Outcome Measures

Name	Time	Method

Locations (1): MS Clinical Research Pvt Ltd
🇮🇳
Bangalore, KARNATAKA, India
MS Clinical Research Pvt Ltd
🇮🇳Bangalore, KARNATAKA, India
Dr Rachana Shilpakr
Principal investigator
08040917253
rachana.shilpakar@mscr.in