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NCT00508976 · ClinicalTrials.gov registry record · Phase 2
Clinical Proposal for the Comparison of Intraperitoneal Anesthetic to Injected Local Anesthetic
A Phase 2 study of Pain, Postoperative and Morbid Obesity, sponsored by Pinnacle Health System.
- Completed
- Registry status
- Phase 2
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT00508976: Completed Phase 2 study of Pain, Postoperative and Morbid Obesity, sponsored by Pinnacle Health System.
NCT00508976 is a Phase 2 study of Pain, Postoperative and Morbid Obesity that has completed, run by Pinnacle Health System. The registered enrollment target is 100 participants, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00508976, a Phase 2 study of Pain, Postoperative and Morbid Obesity, has completed, sponsored by Pinnacle Health System.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine if pre-incisional lidocaine injection, instilled liquid bupivacaine, intra-abdominal aerosolized bupivacaine, or post-operative bupivacaine injection is superior in post-operative pain control in laparoscopic bariatric surgical patients.
Conditions Studied
Interventions
- DRUG Injected bupivacaine post-operatively
- DRUG Streamed bupivacaine versus streamed normal saline
- DRUG Aerosolized bupivacaine versus aerosolized saline
- DRUG Injected lidocaine pre-incision vs saline pre-incision
Study Locations (1)
Pennsylvania
- Pinnacle Health; Community General Osteopathic Hospital - Harrisburg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2007-06 |
| Est. Completion | 2008-04 |
| Phase | Phase 2 |
What the finished NCT00508976 record still lists
NCT00508976 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 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (63% lower).
The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 4 interventions - of which Injected bupivacaine post-operatively is the first listed.
NCT00508976 reports a single indexed study location in Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT00508976 about?
NCT00508976 is a clinical study titled "Clinical Proposal for the Comparison of Intraperitoneal Anesthetic to Injected Local Anesthetic". The purpose of this study is to determine if pre-incisional lidocaine injection, instilled liquid bupivacaine, intra-abdominal aerosolized bupivacaine, or post-operative bupivacaine injection is superior in post-operative pain control in laparoscopic bariatric surgical patients.
What is the current status of trial NCT00508976?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2007-06. Estimated completion is 2008-04.
What conditions does trial NCT00508976 study?
This clinical trial studies the following conditions: Pain, Postoperative, Morbid Obesity.
What interventions are being tested in trial NCT00508976?
The interventions under investigation include: Injected bupivacaine post-operatively (DRUG), Streamed bupivacaine versus streamed normal saline (DRUG), Aerosolized bupivacaine versus aerosolized saline (DRUG), Injected lidocaine pre-incision vs saline pre-incision (DRUG).
Who is sponsoring clinical trial NCT00508976?
This trial is sponsored by Pinnacle Health System, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00508976 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pain, Postoperative
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00508976's enrollment target sits among peer trials
100 44th of 113 higher than 67 of 113 other Pain, Postoperative trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain, Postoperative trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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