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NCT00305396 · ClinicalTrials.gov registry record · Phase 4

Calcineurin Inhibitor Avoidance With Thymoglobulin and Sirolimus in Kidney Transplantation

A Phase 4 study of Kidney Transplantation, sponsored by Vanderbilt University.

Completed
Registry status
Phase 4
Development phase
80
Enrollment target
1
Study location

NCT00305396 is a Phase 4 study of Kidney Transplantation that has completed, run by Vanderbilt University. The registered enrollment target is 80 participants, below the 266-participant average among 33 other Kidney Transplantation trials with a reported enrollment target (70% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00305396, a Phase 4 study of Kidney Transplantation, has completed, sponsored by Vanderbilt University.

COMPLETED
Registry status
Phase 4
Development phase
80 participants
Enrollment target
1
Study location

Study Summary

A prospective, single center, open-label, randomized trial of Thymoglobulin induction and sirolimus, prednisone, and mycophenolate mofetil versus Thymoglobulin induction and tacrolimus, prednisone, and mycophenolate mofetil in non-HLA identical living or deceased donor kidney transplant recipients.

Conditions Studied

Interventions

  • DRUG Sirolimus

Study Locations (1)

Tennessee

  • Vanderbilt University Medical Center/Nashville VA - Nashville

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2004-04
Est. Completion 2005-03
Phase Phase 4

Sponsor

Vanderbilt University

430 total trials

What the Registry Record Tells You About NCT00305396

The ClinicalTrials.gov registry entry for NCT00305396 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 266-participant average among 33 other Kidney Transplantation trials with a reported enrollment target (70% lower). The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Kidney Transplantation appearing as the primary indexed condition, and to 1 intervention - of which Sirolimus is the first listed.

NCT00305396 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.

Frequently Asked Questions

What is clinical trial NCT00305396 about?

NCT00305396 is a clinical study titled "Calcineurin Inhibitor Avoidance With Thymoglobulin and Sirolimus in Kidney Transplantation". A prospective, single center, open-label, randomized trial of Thymoglobulin induction and sirolimus, prednisone, and mycophenolate mofetil versus Thymoglobulin induction and tacrolimus, prednisone, and mycophenolate mofetil in non-HLA identical living or deceased donor kidney transplant recipients.

What is the current status of trial NCT00305396?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 80 participants. The study started on 2004-04. Estimated completion is 2005-03.

What conditions does trial NCT00305396 study?

This clinical trial studies the following conditions: Kidney Transplantation.

What interventions are being tested in trial NCT00305396?

The interventions under investigation include: Sirolimus (DRUG).

Who is sponsoring clinical trial NCT00305396?

This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00305396 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.