Rosacea and Ivermectin

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

April 16, 2021

Primary Completion Date

November 30, 2025

Study Completion Date

December 31, 2025

Conditions
Rosacea
Interventions
DRUG

ivermectin

Subjects will be given the ivermectin with an electronic monitoring device attached with a return appointment at month 3 for end of study visit. Subjects will be instructed to use the ivermectin once daily.

BEHAVIORAL

digital interaction

Subjects will receive weekly digital interaction; an electronic survey asking about their use of the ivermectin which will have the electronic monitoring device attached. Subjects will be instructed to use the ivermectin once daily. They will have a 3 month return appointment for end of study visit.

DEVICE

GPSkin

Subjects in the GPSkin group will receive the GPSkin Barrier® to measure their moisture level of their face daily. Subjects will be instructed to use the ivermectin with the electronic monitoring device once daily. They will be scheduled for a 3 month end of study visit.

Trial Locations (1)

27104

Wake Forest Health Sciences Dermatology, Winston-Salem

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Galderma R&D

INDUSTRY

lead

Wake Forest University Health Sciences

OTHER