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Sequential Compression Devices for Treatment of Restless Legs Syndrome

NCT00479531 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2007-11-30

No results posted yet for this study

Summary

The purpose of this study is to determine if sequential compression devices (SCD) when worn for an hour per day by patients suffering from Restless Legs Syndrome (RLS) are helpful for the improvement of the RLS symptoms and sleep.

Conditions

  • Restless Legs Syndrome

Interventions

DEVICE

AirCast Sequential Compression Device

Sponsors & Collaborators

  • AirCast LLC

    collaborator INDUSTRY

  • Walter Reed Army Medical Center

    lead FED

Principal Investigators

  • Christopher Lettieri, MD · Pulmonary & Critical Care Medicine Service, Walter Reed Army Medical Center, Washington DC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Completion
2007-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00479531 on ClinicalTrials.gov