To check efficacy of wundschutzgel in sunbur
- Conditions
- Health Condition 1: T231- Burn of first degree of wrist andhand
- Registration Number
- CTRI/2022/09/045569
- Lead Sponsor
- TRIN GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1.Age from 18 to 65 years
2.If female with childbearing potential, must be willing to practice an acceptable form of birth control for the duration of the study.
3.Subjects that are able to give written informed consent in a manner approved by the institutional ethics committee and comply with the requirements of the study.
4.Subjects willing to avoid participation in any other interventional clinical trial for the duration of the study.
1.Females that are pregnant, breast feeding, or planning to get pregnant during the study.
2.Patients that have participated in any other interventional clinical trial in the previous 30 days.
3.Patients with known sensitivity to any of the constituents of the investigational product.
4.Any person suffering from heavily bleeding or weeping wound.
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in Sunburn measured as change in VAS ScoreTimepoint: Baseline (day 0) and Day 5
- Secondary Outcome Measures
Name Time Method Change in skin ElasticityTimepoint: Baseline (day 0) and Day 5;Change in skin ErythemaTimepoint: Baseline (day 0) and Day 5;QOL changes to be measured as DLQITimepoint: Baseline (day 0) and Day 5