drugset / Trial / NCT04275999

Rosacea and Ivermectin

NCT04275999

RandomizedParallel-groupOpen-labelHealth-services research

Summary

The primary hypothesis is that weekly digital interactions and routine measurement of Transepidermal Water Loss (TEWL) rates and Subcutaneous hydration levels will promote patient adherence to maintenance ivermectin therapy and prevent disease relapse. The project will consist of a trial in which thirty subjects with rosacea receive ivermectin therapy and are randomized to receive either no intervention, a weekly digital survey to assess patient's attitudes towards ivermectin therapy, or a portal hydration measurement device that measures TEWL rates and SC hydration levels. The study team will measure adherence objectively in all groups with electronic monitors attached to the containers of the ivermectin, which all subjects will be told to use daily for maintenance therapy. Additionally, the hydration measurement device can transmit data to an Internet server via a smartphone using Bluetooth technology, thereby allowing providers to monitor a patient's TEWL rate and SC levels.

Timeline

Start
2021-04-16
Primary completion
2024-01-17
Completion
2025-01-17

Drugs

EvaluationDrugModalityDoseRoute
Background Ivermectin Small molecule

Indications