Ignite Creation Date:
2024-05-06 @ 8:26 PM
Last Modification Date:
2024-10-26 @ 3:27 PM
Study NCT ID:
NCT06384092
Status:
COMPLETED
Last Update Posted:
2024-04-29
First Post:
2024-02-06
Brief Title:
Process Validation in Dermatology Assessing Methods for UV Exposure Artificial Source vs Sunlight and Efficacy Evaluation of Anti-Tanning Agents
Sponsor:
NovoBliss Research Pvt Ltd
Organization:
NovoBliss Research Pvt Ltd
Study Overview
Official Title:
Standardization of UV Exposure Methods Artificial Source vs Sunlight in Dermatological Research A Comprehensive Investigation Into the Efficacy Assessment Methodology for Anti-tanning Agents Through Process Validation
Status:
COMPLETED
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The rationale of this study is to establish a robust method for assessing sun protection product efficacy in preventing erythema and tanning Employing both artificial ultraviolet-A Irradiation and natural direct sunlight exposure the investigation seeks to provide a reliable methodology ensuring reproducibility and enabling a direct comparison between these methods Meticulously determining optimal UV dosages the study prioritizes inducing skin responses for evaluation while avoiding adverse effects like blistering The localized validation of UV exposure techniques tailored to the Indian population contributes significantly to the field by addressing diverse skin types and environmental conditions By incorporating both artificial and natural direct sunlight UV exposure methods the study aspires to enhance the safety and effectiveness of future dermatological investigations benefiting both the scientific community and the broader population
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None