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Process Validation in Dermatology: Assessing Wound Creation Methods and Treatment Efficacy

NCT06379516 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2024-06-27

No results posted yet for this study

Summary

The primary objective of this study is to validate controlled methods of wound, including 1%w/v SLS, 3%w/v SLS, and 24-24 times tape stripping, on the forearms of subjects.

The study aims to standardize the procedures for creating wounds and systematically evaluate the effects of these methods on various skin parameters.

Conditions

  • Validation of the Process of Wound Creation and Evaluation

Interventions

OTHER

Moisturising Cream (5%)

This intervention is a moisturiging cream of concentration 5% for topical application to the respective test sites.

OTHER

Moisturising Cream (10%)

This intervention is a moisturiging cream of concentration 10% for topical application to the respective test sites.

OTHER

Coconut Oil

This intervention is a 100% pure coconut oil product (Parachute Pure Coconut Oil) for topical application to the respective test sites.

Sponsors & Collaborators

  • NovoBliss Research Pvt Ltd

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-17
Primary Completion
2024-01-26
Completion
2024-02-16

Countries

  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06379516 on ClinicalTrials.gov