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NCT00425126 · ClinicalTrials.gov registry record · Phase 4

Effect of Procrit (Epoetin Alfa) on Preventing Delayed Graft Function After Deceased Donor Renal Transplantation

A Phase 4 study of Delayed Graft Function, sponsored by West Penn Allegheny Health System.

Completed
Registry status
Phase 4
Development phase
76
Enrollment target
1
Study location

NCT00425126: Completed Phase 4 study of Delayed Graft Function, sponsored by West Penn Allegheny Health System.

NCT00425126 is a Phase 4 study of Delayed Graft Function that has completed, run by West Penn Allegheny Health System. The registered enrollment target is 76 participants, below the 362-participant average among 6 other Delayed Graft Function trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00425126, a Phase 4 study of Delayed Graft Function, has completed, sponsored by West Penn Allegheny Health System.

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

Study Summary

Delayed graft function (DGF) is a major complication following deceased donor renal transplantation. The surgical procedure of harvesting a kidney from a cadaveric donor and implanting the kidney into the recipient inevitably causes some amount of injury. While not always clinically significant, anywhere from 10-50% of transplant patients may develop DGF. Ongoing research in animal models has demonstrated benefit with administration of erythropoietin. The investigators propose to study the effect of Procrit(Epoetin Alfa) on delayed graft function in subjects undergoing kidney transplantation.

Conditions Studied

Interventions

  • DRUG Epoetin Alfa

Study Locations (1)

Pennsylvania

  • Allegheny General Hospital - Pittsburgh

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2007-02
Est. Completion 2010-02
Phase Phase 4
West Penn Allegheny Health System

14 total trials

What the finished NCT00425126 record still lists

NCT00425126 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 362-participant average among 6 other Delayed Graft Function trials with a reported enrollment target (79% lower).

The record links to 1 condition, with Delayed Graft Function appearing as the primary indexed condition, and to 1 intervention - of which Epoetin Alfa is the first listed.

NCT00425126 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00425126 about?

NCT00425126 is a clinical study titled "Effect of Procrit (Epoetin Alfa) on Preventing Delayed Graft Function After Deceased Donor Renal Transplantation". Delayed graft function (DGF) is a major complication following deceased donor renal transplantation. The surgical procedure of harvesting a kidney from a cadaveric donor and implanting the kidney into the recipient inevitably causes some amount of injury. While not always clinically significant, any...

What is the current status of trial NCT00425126?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 76 participants. The study started on 2007-02. Estimated completion is 2010-02.

What conditions does trial NCT00425126 study?

This clinical trial studies the following conditions: Delayed Graft Function.

What interventions are being tested in trial NCT00425126?

The interventions under investigation include: Epoetin Alfa (DRUG).

Who is sponsoring clinical trial NCT00425126?

This trial is sponsored by West Penn Allegheny Health System, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00425126 being conducted?

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

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Source: ClinicalTrials.gov NCT00425126, the US trial registry maintained by the National Library of Medicine. NCT00425126 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.