12-week Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome
Status: | Completed |
---|---|
Conditions: | Restless Leg Syndrome, Neurology |
Therapuetic Areas: | Neurology, Rheumatology |
Healthy: | No |
Age Range: | 18 - 79 |
Updated: | 10/14/2017 |
Start Date: | October 2006 |
End Date: | June 2007 |
A 12-Week, Multi-Center, Double-Blind, Placebo-Controlled, Parallel Group, Flexible Dose Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome (RLS) in RLS Patients With Sleep Disturbance and Periodic Limb Movements (PLM) During Sleep
The purpose of this study is to assess the efficacy and safety of ropinirole CR-RLS in the
treatment of patients with Restless Legs Syndrome and associated sleep disturbance and period
limb movements during sleep.
treatment of patients with Restless Legs Syndrome and associated sleep disturbance and period
limb movements during sleep.
Inclusion criteria:
- provided written informed consent.
- Diagnosed with primary RLS using the International RLS Study Group Diagnostic Criteria
with a total score of 20 or greater on the International RLS (IRLS) Rating Scale and
significant sleep disturbance indicated on Item 4 of the IRLS rating scale.
- Have evening and nighttime symptoms of RLS, significant sleep impairment due to RLS
symptoms, and symptoms requiring treatment prior to bedtime, but no earlier than
5:00PM.
- Sleep efficiency <85% OR Latency to persistent sleep >20 minutes.
Exclusion criteria:
- Secondary RLS
- Primary sleep disorder
- Have any medical conditions that may impact efficacy assessments or that may present a
safety concern.
- Pregnant or lactating or women of child-bearing potential who are not practicing an
acceptable method of birth control.
- Use of any prohibited medication.
We found this trial at
44
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