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A Self-Controlled Study on the Treatment of Restless Legs Syndrome in Uremia With Dipyridamole
Sponsor: Yunfeng Xia
Summary
The purpose of this clinical trial is to determine whether dipyridamole can treat restless legs syndrome in patients with uremia. In addition, the safety of dipyridamole will also be evaluated. The main questions this study aims to answer include: Can dipyridamole improve the symptoms of restless legs syndrome in participants? Can dipyridamole improve participants' anxiety, depression, sleep quality, and quality of life? What adverse reactions might participants experience while taking dipyridamole? This study is a self-controlled trial in which all participants receive active drug treatment. Participants will take dipyridamole daily (50 mg per dose, three times a day) for 6 months. The efficacy of dipyridamole will be evaluated by comparing relevant scale scores and laboratory indicators before and after treatment. In addition, adverse reactions during the treatment follow-up will be monitored to assess the safety of dipyridamole in this patient population.
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
80
Start Date
2025-07-01
Completion Date
2026-12-31
Last Updated
2025-10-07
Healthy Volunteers
No
Conditions
Interventions
Dipyridamole 50mg tid
Participants will take dipyridamole daily (50mg each time, three times a day) for 6 months
Locations (1)
First Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality, China