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

NCT00459602 · ClinicalTrials.gov registry record

Incisional Hernia Outcomes Study Using Parietex Composite Mesh

A clinical trial, sponsored by Columbia University.

Terminated
Registry status
22
Enrollment target

NCT00459602: Clinical Trial study, sponsored by Columbia University.

NCT00459602 is a clinical trial that was terminated before completion, run by Columbia University. The registered enrollment target is 22 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00459602 was terminated before completion, sponsored by Columbia University.

TERMINATED
Registry status
22 participants
Enrollment target

Study Summary

The purpose of this study is to describe the outcomes of laparoscopic incisional hernia repair surgery and to record the outcomes of patients after surgery.

Primary Outcome

pain assessment

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2004-08
Est. Completion 2008-09
Columbia University

958 total trials

Why NCT00459602 stopped before completion

NCT00459602 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 22 participants, a relatively small participant target.

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

NCT00459602 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00459602 about?

NCT00459602 is a clinical study titled "Incisional Hernia Outcomes Study Using Parietex Composite Mesh". The purpose of this study is to describe the outcomes of laparoscopic incisional hernia repair surgery and to record the outcomes of patients after surgery.

What is the current status of trial NCT00459602?

This trial is currently terminated. The enrollment target is 22 participants. The study started on 2004-08. Estimated completion is 2008-09.

Who is sponsoring clinical trial NCT00459602?

This trial is sponsored by Columbia University, which has 958 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

  • NCT02508038 · 22 participants · Phase 1

    Alpha/Beta CD19+ Depleted Haploidentical Transplantation + Zometa for Pediatric Hematologic Malignancies and Solid Tumors

  • NCT03099356 · 22 participants · Phase 2

    Cyclophosphamide and Sirolimus for the Treatment of Metastatic, RAI-refractory, Differentiated Thyroid Cancer

  • NCT03676647 · 22 participants

    Diagnostic DNA Methylation Signature in Diagnosing Thyroid Cancer After Fine-Needle Aspiration in Patients With Thyroid Nodules

  • NCT04569591 · 22 participants · NA

    DDAVP for Pituitary Adenoma

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 NCT00459602, the US trial registry maintained by the National Library of Medicine. NCT00459602 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.