Health Condition 1: T231- Burn of first degree of wrist andhand
Conditions
Interventions
Intervention1: Wundschutzgel gel: Dose: approx 1ml twice a day route of administration: Topical
duration: 5 days
Control Intervention1: Not Applicable: Not Applicable
Sponsors
NUTRIN GmbH
Mittal Global Clinical Trial Services
Eligibility
Inclusion criteria
Inclusion criteria: 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.
Exclusion criteria
Exclusion criteria: 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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in Sunburn measured as change in VAS ScoreTimepoint: Baseline (day 0) and Day 5 | — |
Secondary
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
India
Contacts
Public ContactPuneet Mittal
Mittal Global Clinical Trial Services
Outcome results
None listed