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NCT00472134 · ClinicalTrials.gov registry record · NA
Laparoscopic Ventral Hernia Repair With Elastomeric Pain Pump
A NA study of Hernia, Ventral, sponsored by University Hospitals Cleveland Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT00472134: Completed NA study of Hernia, Ventral, sponsored by University Hospitals Cleveland Medical Center.
NCT00472134 is a NA study of Hernia, Ventral that has completed, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 100 participants, below the 169-participant average among 7 other Hernia, Ventral trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00472134, a NA study of Hernia, Ventral, has completed, sponsored by University Hospitals Cleveland Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the effects of a local anesthetic dispensed via a tiny catheter device, called the ON-Q PainBuster pump, placed during surgery on top of the mesh used in the laparoscopic repair of ventral hernias. The goals are: * reducing postoperative pain from this procedure * decreasing length of hospital stay * reducing or eliminating amount of post-operative narcotics used
Conditions Studied
Interventions
- DRUG bupivacaine
- DEVICE On-Q PainBuster pump
Study Locations (1)
Ohio
- University Hospitals of Cleveland - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2005-12 |
| Est. Completion | 2007-12 |
| Phase | NA |
What the finished NCT00472134 record still lists
NCT00472134 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 169-participant average among 7 other Hernia, Ventral trials with a reported enrollment target (41% lower).
The record links to 1 condition, with Hernia, Ventral appearing as the primary indexed condition, and to 2 interventions - of which bupivacaine is the first listed.
NCT00472134 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT00472134 about?
NCT00472134 is a clinical study titled "Laparoscopic Ventral Hernia Repair With Elastomeric Pain Pump". The purpose of this study is to determine the effects of a local anesthetic dispensed via a tiny catheter device, called the ON-Q PainBuster pump, placed during surgery on top of the mesh used in the laparoscopic repair of ventral hernias. The goals are: * reducing postoperative pain from this proc...
What is the current status of trial NCT00472134?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2005-12. Estimated completion is 2007-12.
What conditions does trial NCT00472134 study?
This clinical trial studies the following conditions: Hernia, Ventral.
What interventions are being tested in trial NCT00472134?
The interventions under investigation include: bupivacaine (DRUG), On-Q PainBuster pump (DEVICE).
Who is sponsoring clinical trial NCT00472134?
This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00472134 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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