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NCT00360477 · ClinicalTrials.gov registry record · NA

FloSeal Tubeless Exit Versus Cope Loop Nephrostomy Versus Fascial Stitch Following Percutaneous Nephrolithotripsy

A NA study, sponsored by University of California, Irvine.

Completed
Registry status
NA
Development phase
59
Enrollment target

NCT00360477 is a NA study that has completed, run by University of California, Irvine. The registered enrollment target is 59 participants.

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The verdict

NCT00360477, a NA study, has completed, sponsored by University of California, Irvine.

COMPLETED
Registry status
NA
Development phase
59 participants
Enrollment target

Study Summary

The patient will be asked to participate in a research project designed to determine the best way to prevent bleeding and promote patient comfort after having kidney stones removed. Two standard methods for ending the surgery are being compared to a newer method. In one standard method, the patient will have a tube draining urine from the kidney after the procedure. This tube may also prevent bleeding from the kidney. In another standard method the patient will have a tube left internally that drains urine from the kidney to the bladder and a stitch will be used to close the incision and deeper tissues in the back. In the third potential option, a tube would be left internally to drain urine from the kidney to the patient's bladder and the surgical site would be filled with a clot promoting agent (FloSeal) which is a FDA approved agent specifically formulated to stop bleeding during surgical procedures.

Interventions

  • PROCEDURE Floseal
  • PROCEDURE Cope Loop
  • PROCEDURE Fascial Stitch

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2004-06
Est. Completion 2015-01
Phase NA

Sponsor

University of California, Irvine

368 total trials

What the Registry Record Tells You About NCT00360477

The ClinicalTrials.gov registry entry for NCT00360477 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 59 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Irvine, which has 368 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Floseal is the first listed.

NCT00360477 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00360477 about?

NCT00360477 is a clinical study titled "FloSeal Tubeless Exit Versus Cope Loop Nephrostomy Versus Fascial Stitch Following Percutaneous Nephrolithotripsy". The patient will be asked to participate in a research project designed to determine the best way to prevent bleeding and promote patient comfort after having kidney stones removed. Two standard methods for ending the surgery are being compared to a newer method. In one standard method, the patient ...

What is the current status of trial NCT00360477?

This trial is currently completed. It is a NA study. The enrollment target is 59 participants. The study started on 2004-06. Estimated completion is 2015-01.

What interventions are being tested in trial NCT00360477?

The interventions under investigation include: Floseal (PROCEDURE), Cope Loop (PROCEDURE), Fascial Stitch (PROCEDURE).

Who is sponsoring clinical trial NCT00360477?

This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.

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

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.