CClinicalTrials.gg
CompletedNCT02025608AUTORESTUpdated Jan 24, 2017

Autonomic Function and Cardiovascular Risk in Restless Legs Syndrome

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

Phase
Phase 4
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
30 Years to 65 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Restless Legs Syndrome

Keywords

  • Restless legs syndrome
03

In context

Psychomotor Agitation

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
30 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Willingness to participate and written informed consent
  • Aged 30 to 65 years at the time of screening
  • Body mass index (BMI) ≤ 30
  • Unremarkable neurological and physical examination
  • Unremarkable standard blood parameter according to local reference values

Additional Inclusion Criteria for Restless Legs Syndrome (RLS) Patients:

  • RLS according to current standard international criteria
  • RLS symptoms ≥ 2 times per week for ≥ 1 year and during the past 12 months.
  • Either current international RLS severity scale (IRLS) ≥ 15 or current IRLS ≥ 10 and RLS symptoms ≥ 4 times per week during the past 3 months.

Exclusion criteria

Exclusion Criteria (all participants):

  • Pregnancy, or breast feeding at time of screening.
  • Recent anaesthesia (last 3 months).
  • Sleep related breathing disorders during nocturnal polysomnography:
  • Current history of psychiatric disorders according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV).
  • Life time history of any diagnosis of, medication or intervention for cardiovascular diseases.
  • Current chronic treatment that may affect autonomic function.
  • Any significant neurological disease or diagnosed metabolic diseases that may affect cardiovascular function and/or increase cardiovascular risk.
  • Any unstable medical condition.
  • Smoking > 5 cigarettes per day during the last 2 years.
  • Work involving night shifts (22:00 - 06:00 h) during the past 2 years.
  • Travel with > 6 time zone differences during the past 6 months.
  • Participation in any other study involving investigational or marketed products concomitantly or within 3 months prior to the screening visit.
  • Current participation in other clinical trials.

Additional Exclusion Criteria for RLS Patients

  • Exposure to dopaminergic drugs > 12 months during life time and/or > 1 week during the past 3 months and/or current or during the past month.
  • Exposure to other RLS relevant medication (such as opioids, antiepileptics, clonidine except hypnotics such as benzodiazepines) > 24 months during life time and/or > 1 week during the past 3 months and/or current intake.
  • Intake of hypnotics (such as benzodiazepines) during the past month.
  • Other significant sleep disorder except symptoms potentially related to RLS such as insomnia and daytime sleepiness.
  • Any contraindication or known hypersensitivity to dopaminergic drugs.

Additional Exclusion Criteria for Control Subjects

  • Any pharmacological treatment that may affect sleep and/or sleep related movement disorders during the last 3 months.
  • Any clinically significant sleep disorders according to the International Classification of Sleep Disorders (ICSD)12.
  • Increased daytime sleepiness as indicated by an Epworth Sleepiness Scale (ESS) score > 11.
05

Study design

Phase
Phase 4
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Pramipexole

    Pramipexole, 0.25 mg, daily for 4 weeks

    Drug: Pramipexole

  • Placebo comparator
    Placebo

    Placebo, daily for 4 weeks

    Drug: Placebo

Interventions

  • DrugPramipexole
  • DrugPlacebo
06

What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. Change in baroreflex from baseline to 4 weeks

    Baroreflex sensitivity and baroreflex gain derived from tilt table tes

    Time frame: Baseline, Week 4

  2. 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

Other outcomes

  1. 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

07

Study locations

2 sites
  • Neurocenter of Southern Switzerland
    Lugano, Ticino 6903, Switzerland
  • Department of Neurology, Inselspital
    Bern, 3010, Switzerland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 24, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02025608
Lead sponsor
Mauro Manconi
Collaborators
Insel Gruppe AG, University Hospital Bern, Cardiocentro Ticino
Responsible party
Mauro Manconi (Dr. med., Ospedale Regionale di Lugano) — Sponsor-investigator
First posted
Jan 1, 2014
Start date
Dec 2013
Primary completion
Dec 31, 2016
Completion
Dec 31, 2016
Last update
Jan 24, 2017

Study contacts

Mauro Manconi, PhD, MD
principal investigator · Neurocenter of Southern Switzerland
Claudio L.A. Bassetti, MD
principal investigator · Department of Neurology, Inselspital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion