Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00228176 · ClinicalTrials.gov registry record · Phase 3

Atherosclerosis Underlying Development Assessed by Intima-Media Thickness in Patients on Rimonabant

A Phase 3 study, sponsored by Sanofi.

Terminated
Registry status
Phase 3
Development phase
661
Enrollment target

NCT00228176: Clinical Trial Phase 3 study, sponsored by Sanofi.

NCT00228176 is a Phase 3 study that was terminated before completion, run by Sanofi. The registered enrollment target is 661 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (14% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00228176, a Phase 3 study, was terminated before completion, sponsored by Sanofi.

TERMINATED
Registry status
Phase 3
Development phase
661 participants
Enrollment target

Study Summary

Objectives: * Primary: To evaluate the effect of rimonabant 20-mg once daily in comparison with placebo, on the quantitative progression of atherosclerosis as assessed by carotid artery intima-media thickness (CIMT) * Secondary: To evaluate the safety and tolerability of the above rimonabant regimen in the study population of atherosclerosis patients.

Interventions

  • DRUG Rimonabant
  • DRUG Placebo (for Rimonabant)

Trial Details

FieldValue
Enrollment Target 661 participants
Start Date 2005-08
Est. Completion 2009-04
Phase Phase 3
Sanofi

713 total trials

Why NCT00228176 stopped before completion

NCT00228176 is an interventional study that assigns participants to a tested intervention. The registered 661 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (14% lower).

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

NCT00228176 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00228176 about?

NCT00228176 is a clinical study titled "Atherosclerosis Underlying Development Assessed by Intima-Media Thickness in Patients on Rimonabant". Objectives: * Primary: To evaluate the effect of rimonabant 20-mg once daily in comparison with placebo, on the quantitative progression of atherosclerosis as assessed by carotid artery intima-media thickness (CIMT) * Secondary: To evaluate the safety and tolerability of the above rimonabant regime...

What is the current status of trial NCT00228176?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 661 participants. The study started on 2005-08. Estimated completion is 2009-04.

What interventions are being tested in trial NCT00228176?

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

Who is sponsoring clinical trial NCT00228176?

This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00228176's enrollment target sits among peer trials

661 556th of 2000 higher than 1,445 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05254743 · 662 participants · Phase 3

    A Study of Pirtobrutinib (LOXO-305) Versus Ibrutinib in Participants With Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

  • NCT01185132 · 660 participants · Phase 3

    Intensity Modulated Radiotherapy (IMRT) vs. 3D-conformal Accelerated Partial Breast Irradiation (APBI) for Early Stage Breast Cancer After Lumpectomy

  • NCT03346694 · 660 participants · NA

    Reducing Surgical Site Infection Rates Using an Alternative Sternal Dressing

  • NCT05407636 · 660 participants · Phase 3

    Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00228176, the US trial registry maintained by the National Library of Medicine. NCT00228176 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.