A Phase 4 interventional study of Pramipexole and Placebo in Restless Legs Syndrome, sponsored by Mauro Manconi. Completed at 2 sites in Switzerland. Open to participants aged 30 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-01-24.
Sponsored by Mauro Manconi · Phase 4, Interventional, and Other
The purpose of this study is to explore whether patients with restless legs syndrome (RLS) differ from healthy subjects in daytime and night time autonomic function and cardiovascular risk markers and whether 4 week treatment with pramipexole affects autonomic function and cardiovascular risk markers in patients with RLS.
500 studies on the registry are indexed under Psychomotor Agitation; 55 are open to participants now.
This study's enrollment of 20 is below the median of 90 across 413 interventional studies indexed under Psychomotor Agitation.
Browse Psychomotor Agitation studies →Mauro Manconi is the lead sponsor of 3 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Additional Inclusion Criteria for Restless Legs Syndrome (RLS) Patients:
Exclusion Criteria (all participants):
Additional Exclusion Criteria for RLS Patients
Additional Exclusion Criteria for Control Subjects
Pramipexole, 0.25 mg, daily for 4 weeks
Drug: Pramipexole
Placebo, daily for 4 weeks
Drug: Placebo
Change in heart rate activations during sleep from baseline to 4 weeks
Number and amplitude of periodic leg movements during sleep (PLMS) and non-PLMS related heart rate activations during stable nocturnal sleep
Time frame: Baseline, Week 4
Change in baroreflex from baseline to 4 weeks
Baroreflex sensitivity and baroreflex gain derived from tilt table tes
Time frame: Baseline, Week 4
Change in blood serum markers from baseline to 4 weeks
Highly-sensitive C reactive protein (hsCRP), lipoprotein-associated phospholipase A2 (lP-PLA2), and oxidised low density lipoprotein (oxLDL)
Time frame: Baseline, Week 4
Change in chemoreflexes from baseline to 4 weeks
Peripheral and central chemoreflex sensitivity derived from carbon dioxide (CO2) rebreathing test
Time frame: Baseline, Week 4
This study is completed, as verified in Jan 2017. You cannot join it, but the record below documents what was studied.
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