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NCT00479531 · ClinicalTrials.gov registry record · Phase 3

Sequential Compression Devices for Treatment of Restless Legs Syndrome

A Phase 3 study, sponsored by Walter Reed Army Medical Center.

Completed
Registry status
Phase 3
Development phase
40
Enrollment target

NCT00479531: Completed Phase 3 study, sponsored by Walter Reed Army Medical Center.

NCT00479531 is a Phase 3 study that has completed, run by Walter Reed Army Medical Center. The registered enrollment target is 40 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00479531, a Phase 3 study, has completed, sponsored by Walter Reed Army Medical Center.

COMPLETED
Registry status
Phase 3
Development phase
40 participants
Enrollment target

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.

Interventions

  • DEVICE AirCast Sequential Compression Device

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2005-09
Est. Completion 2007-10
Phase Phase 3
Walter Reed Army Medical Center

24 total trials

What the finished NCT00479531 record still lists

NCT00479531 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which AirCast Sequential Compression Device is the first listed.

NCT00479531 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00479531 about?

NCT00479531 is a clinical study titled "Sequential Compression Devices for Treatment of Restless Legs Syndrome". 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.

What is the current status of trial NCT00479531?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 40 participants. The study started on 2005-09. Estimated completion is 2007-10.

What interventions are being tested in trial NCT00479531?

The interventions under investigation include: AirCast Sequential Compression Device (DEVICE).

Who is sponsoring clinical trial NCT00479531?

This trial is sponsored by Walter Reed Army Medical Center, which has 24 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00479531's enrollment target sits among peer trials

40 1878th of 2000 higher than 103 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00479531, the US trial registry maintained by the National Library of Medicine. NCT00479531 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.