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NCT00109772 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Efficacy and Safety of Lenalidomide in the Treatment of Complex Regional Pain Syndrome Type 1

A Phase 2 study, sponsored by Celgene Corporation.

Terminated
Registry status
Phase 2
Development phase
184
Enrollment target

NCT00109772: Clinical Trial Phase 2 study, sponsored by Celgene Corporation.

NCT00109772 is a Phase 2 study that was terminated before completion, run by Celgene Corporation. The registered enrollment target is 184 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (38% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00109772, a Phase 2 study, was terminated before completion, sponsored by Celgene Corporation.

TERMINATED
Registry status
Phase 2
Development phase
184 participants
Enrollment target

Study Summary

The purpose of this multicenter, double-blind, placebo-controlled study is to evaluate the efficacy and safety of Lenalidomide in adult subjects with Complex Regional Pain Syndrome (CRPS) Type 1.

Primary Outcome

Participants rated the intensity of pain in the CRPS-affected limb twice each day in a diary. The PI-NRS is an eleven point scale with 0=no pain and 10=worst pain imaginable. Responders are participants who completed 12 weeks of treatment and their week 12 PI-NRS score showed at least a 30% improvement from baseline. Participants who did not complete 12 weeks of treatment are considered non-responders.

Interventions

  • DRUG Placebo
  • DRUG lenalidomide

Trial Details

FieldValue
Enrollment Target 184 participants
Start Date 2005-02
Est. Completion 2008-04
Phase Phase 2
Celgene Corporation

40 total trials

Why NCT00109772 stopped before completion

NCT00109772 is an interventional study that assigns participants to a tested intervention. The registered 184 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (38% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00109772 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00109772 about?

NCT00109772 is a clinical study titled "Study to Evaluate the Efficacy and Safety of Lenalidomide in the Treatment of Complex Regional Pain Syndrome Type 1". The purpose of this multicenter, double-blind, placebo-controlled study is to evaluate the efficacy and safety of Lenalidomide in adult subjects with Complex Regional Pain Syndrome (CRPS) Type 1.

What is the current status of trial NCT00109772?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 184 participants. The study started on 2005-02. Estimated completion is 2008-04.

What interventions are being tested in trial NCT00109772?

The interventions under investigation include: Placebo (DRUG), lenalidomide (DRUG).

Who is sponsoring clinical trial NCT00109772?

This trial is sponsored by Celgene Corporation, which has 40 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00109772's enrollment target sits among peer trials

184 360th of 2000 higher than 1,638 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00109772, the US trial registry maintained by the National Library of Medicine. NCT00109772 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.