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

NCT00833430 · ClinicalTrials.gov registry record

Avascular Necrosis (AVN) Long-Term Follow-up

A clinical trial, sponsored by Zimmer Biomet.

Terminated
Registry status
35
Enrollment target

NCT00833430: Clinical Trial study, sponsored by Zimmer Biomet.

NCT00833430 is a clinical trial that was terminated before completion, run by Zimmer Biomet. The registered enrollment target is 35 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00833430 was terminated before completion, sponsored by Zimmer Biomet.

TERMINATED
Registry status
35 participants
Enrollment target

Study Summary

Long-term follow-up of IDE patients for publication

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2006-06
Est. Completion 2013-02
Zimmer Biomet

115 total trials

Why NCT00833430 stopped before completion

NCT00833430 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 35 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT00833430 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00833430 about?

NCT00833430 is a clinical study titled "Avascular Necrosis (AVN) Long-Term Follow-up". Long-term follow-up of IDE patients for publication

What is the current status of trial NCT00833430?

This trial is currently terminated. The enrollment target is 35 participants. The study started on 2006-06. Estimated completion is 2013-02.

Who is sponsoring clinical trial NCT00833430?

This trial is sponsored by Zimmer Biomet, which has 115 total clinical trials registered on ClinicalTrials.gov.

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

  • NCT01697371 · 35 participants · NA

    Proton Therapy in the Treatment of Liver Metastases

  • NCT01940757 · 35 participants · Phase 1

    Experimental Infection of Hookworm-naïve Adults With Dermally-applied Infectious Necator Americanus Hookworm Larvae

  • NCT02235857 · 35 participants · NA

    Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children

  • NCT02637934 · 35 participants · Phase 1

    Phase I Pilot Study of Biodistribution, Metabolism and Excretion of Novel Radiotracer [18F]Fluorthanatrace (FTT) by PET/CT

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 NCT00833430, the US trial registry maintained by the National Library of Medicine. NCT00833430 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.