Primary Irritation Patch Test on Adult Healthy Human Participants with Normal Skin.

Not Applicable

Completed

• Registration Number: CTRI/2023/12/060910
• Lead Sponsor: Dr. Siva Ayush Pharma Services

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2024-01-10
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 25

Inclusion Criteria

1)Males and non-pregnant or non-lactating females preferably equal numbers of males and females between age group of 18 to 65 years both inclusive at the time of consent.

2)Participants with normal Fitzpatrick skin type III to V. Human skin colour determination scale.

3)Females of childbearing potential must have a negative urine pregnancy test performed on Day 01 prior to patch application.

4)Participants who do not have any previous history of adverse skin conditions and are not under any medication are likely to interfere with the results.

5)Participants are in good general health as determined by the Investigator on the basis of medical history.

6)Participants willing to maintain the test patches in designated positions for 24 Hours and refrain from vigorous physical exercise during the study period.

Exclusion Criteria

1)Participants having skin irritation, blemishes, excessive hair, moles, pigmentation, pimples, marks e.g., tattoos, scars, and sunburn), open wounds, cuts, abrasions, irritation symptoms or any dermatological condition on the test sites i.e., back that can interfere with the reading.

2)Participant with history of asthma or COPD Chronic obstructive pulmonary disease, diabetes and mastectomy for cancer involving removal of lymph nodes within the past year, or treatment of any type of cancer within the last 6 months.

3)Participant suffering from any active clinically significant skin diseases which may affect the study results.

4)Participant having history of any skin diseases including eczema, atopic dermatitis.

5)Participation in any patch test for irritation or sensitization within the last four weeks.

6)Participants taking part in another study liable to interfere with the results of this study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified