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Assessment of Varnya Lepa Suncreen Lotion in healthy individuals

Phase 1
Completed
Conditions
Health Condition 1: L599- Disorder of the skin and subcutaneous tissue related to radiation, unspecified
Registration Number
CTRI/2020/09/027895
Lead Sponsor
Dr Shikha
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

1)Healthy Persons should pass skin irritability test.

2)Age group in between 20ââ?¬â??50 years.

3)Willing to give consent for participating in the study.

4)All type of skin color will be included.

Exclusion Criteria

1)History of major medical illness such as Tuberculosis, Cardiac ailments, Bronchial asthma etc.

2)Person who is having severe skin allergy must be excluded.

3)Person who is having severe wound, injury, eczema, leucoderma etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A novel Varnya lepa sunscreen lotion may be prepared, Physico-chemically analyzed and evaluate clinically for safety and efficacyTimepoint: 18 months
Secondary Outcome Measures
NameTimeMethod
To compare the effect of Varnya Lepa Suncreen Lotion with standard Lactocalamine Suncreen lotionTimepoint: 18 months
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