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Completed Phase 2Phase 3 Interventional

Study to Evaluate the Efficacy and Safety of Lenalidomide in the Treatment of Painful Lumbar Radiculopathy

ClinicalTrials.gov ID: NCT00120120

Public ClinicalTrials.gov record NCT00120120. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 6:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Lenalidomide in the Treatment of Painful Lumbar Radiculopathy

Study identification

NCT ID
NCT00120120
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Celgene Corporation
Industry
Enrollment
181 participants

Conditions and interventions

Conditions

Interventions

  • Lenalidomide (CC-5013) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2004
Primary completion
Sep 30, 2007
Completion
Oct 31, 2007
Last update posted
Sep 22, 2009

2005 – 2007

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
Arizona Research Center Phoenix Arizona 85023
Genova Clinical Research, Inc Tucson Arizona 85741
Loma Linda Institution Loma Linda California 92354
Space Coast Neurology Palm Bay Florida 32905
Gold Coast Research, LLC Weston Florida 33331
Emory University Hospital Atlanta Georgia 30322
Rehab Institute of Chicago Chicago Illinois 60611
University of Iowa Iowa City Iowa 52242
Johns Hopkins Pain Center Baltimore Maryland 21205
Mayo Clinic Rochester Minnesota 55905
Washington University Pain Mgmt Ctr St Louis Missouri 63141
North Shore University Hospital Bethpage New York 11554
University of Rochester Medical CenterPain Services Rochester New York 14642
Duke University Medical Center Durham North Carolina 27705
Carolinas Pain Institute, P.A. & the Center for Clinical Research, LLC Winston-Salem North Carolina 27103
Research Institute of Greater Dayton Dayton Ohio 45432
Attn: Maryjane CerroneLehigh Valley Hospital Allentown Pennsylvania 18103-6208
Drexel University College of MedicineDepartment of Neurology Rm 7102 Philadelphia Pennsylvania 19102
Texas Tech Medical Center Department of Anesthesiology Lubbock Texas 79430
KRK Medical Research Richardson Texas 75080
Fletcher Allen Healthcare for Pain Medicine South Burlington Vermont 05403
University of Virginia Pain Management Center Charlottesville Virginia 22903
Swedish Pain Services Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00120120, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 22, 2009 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00120120 live on ClinicalTrials.gov.

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