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NCT01008709 · ClinicalTrials.gov registry record · NA

Comparison Study of Two Different Surgical Clips During Laparoscopic Urologic Surgery

A NA study, sponsored by Vanderbilt University Medical Center.

Terminated
Registry status
NA
Development phase
11
Enrollment target

NCT01008709 is a NA study that was terminated before completion, run by Vanderbilt University Medical Center. The registered enrollment target is 11 participants.

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The verdict

NCT01008709, a NA study, was terminated before completion, sponsored by Vanderbilt University Medical Center.

TERMINATED
Registry status
NA
Development phase
11 participants
Enrollment target

Study Summary

Intracorporeal suturing and knot tying during robotic prostatectomy and laparoscopic and robotic renal surgery have historically been considered the most technically challenging and time consuming aspects of these procedures. With improved operative technique as well as the use of innovative surgical devices, vascular control during these surgeries is often less cumbersome as compared with traditional techniques. Current standard methods of hemostasis include the use of clips, of which the most popular design is the Hemolock, a locking, nonabsorbable plastic clip, or the use of the very expensive endomechanical stapler. Unfortunately while they are associated with time savings in the operating room, there is a great deal of disposable costs associated with these various devices as well as a not insignificant device malfunction rate reported in the literature. The aim of this case-controlled study is to evaluate the Aesculap U-clip device compared to our current technique of vascular control using the Teleflex Hemolock clip device during minimally invasive genitourinary surgery.

Interventions

  • DEVICE Teleflex HemoLock clip
  • DEVICE Aesculap U-clip

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2009-10
Est. Completion 2012-11
Phase NA

What the Registry Record Tells You About NCT01008709

The ClinicalTrials.gov registry entry for NCT01008709 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Teleflex HemoLock clip is the first listed.

NCT01008709 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01008709 about?

NCT01008709 is a clinical study titled "Comparison Study of Two Different Surgical Clips During Laparoscopic Urologic Surgery". Intracorporeal suturing and knot tying during robotic prostatectomy and laparoscopic and robotic renal surgery have historically been considered the most technically challenging and time consuming aspects of these procedures. With improved operative technique as well as the use of innovative surgica...

What is the current status of trial NCT01008709?

This trial is currently terminated. It is a NA study. The enrollment target is 11 participants. The study started on 2009-10. Estimated completion is 2012-11.

What interventions are being tested in trial NCT01008709?

The interventions under investigation include: Teleflex HemoLock clip (DEVICE), Aesculap U-clip (DEVICE).

Who is sponsoring clinical trial NCT01008709?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 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.