NCT04687839View on ClinicalTrials.gov

Assessment of the Wound Healing Efficacy and Tolerance of a Medical Device on Wounds in Healthy Subjects.

NACompletedINTERVENTIONAL
Enrollment

44

Participants

Timeline

Start Date

July 13, 2020

Primary Completion Date

August 17, 2020

Study Completion Date

August 17, 2020

Conditions
Healthy
Interventions
PROCEDURE

Induction of suction blister

For each subject, 2 superficial wounds will be made on the inner aspect of each forearm using the suction blister model.

OTHER

Transepidermal water loss (TEWL)

"* At V1, before blister suction use (T0) and after blister withdrawal before product application (T1)~* For subsequent visits, before product application"

OTHER

Macrophotography

"* At V1, before blister suction use (T0) and after blister withdrawal before product application (T1)~* For subsequent visits, before product application"

DEVICE

Wound healing medical device

Twice daily application on superficial wounds

Trial Locations (1)

22869

Dr. Kirstin Deuble-Bente, Schenefeld

All Listed Sponsors
lead

Pierre Fabre Dermo Cosmetique

INDUSTRY

NCT04687839 - Assessment of the Wound Healing Efficacy and Tolerance of a Medical Device on Wounds in Healthy Subjects. | Biotech Hunter | Biotech Hunter