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COMPLETED
NCT07533474
NA

Human In Use Test of GINPI-HP-004 in Healthy Adults

Sponsor: i+Med S.Coop.

View on ClinicalTrials.gov

Summary

The main objective of this study was to confirm skin acceptability of the product GINPI REF. GINPI BATCH: 10/06/2024 applied under normal use conditions in healthy female adult volunteers, under gynecological control, by means of the evaluation of organoleptic characteristics and subjective efficacy of the study product by the volunteers. Other (secondary) objective was the assessment of unexpected adverse events referred by the volunteers as well as possible reactions observed by the investigator.

Official title: SAFETY HUMAN IN USE TEST UNDER GYNECOLOGICAL CONTROL FOR THE APPRECIATION OF SKIN ACCEPTABILITY OF THE PRODUCT GINPI REF. GINPI BATCH: 10/06/2024 IN HEALTHY FEMALE ADULT VOLUNTEERS

Key Details

Gender

FEMALE

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2024-06-13

Completion Date

2024-07-04

Last Updated

2026-04-16

Healthy Volunteers

Yes

Interventions

OTHER

Depigmentig cosmetic product

Apply the cosmetic product at night, one or two pumps until the area to be treated is covered. Massage the vulvar area until completely absorbed.

Locations (1)

Anmar Clinical Services, S.L.U.

Pamplona, Navarre, Spain