Rosacea and Ivermectin
NCT: NCT04275999 · COMPLETED
Brief 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.
Frequently Asked Questions
What is Rosacea and Ivermectin?
Rosacea and Ivermectin is a clinical trial registered under NCT04275999. Current status: COMPLETED.
What is the status of NCT04275999?
The current status of NCT04275999 (Rosacea and Ivermectin) is: COMPLETED.
When did Rosacea and Ivermectin start?
Rosacea and Ivermectin started on 2021-04-16.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.