Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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 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 108 other Pain, Postoperative trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00508976
The ClinicalTrials.gov registry entry for NCT00508976 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (63% lower). The listed sponsor is Pinnacle Health System, which has 2 total studies on file at ClinicalTrials.gov.
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 1 study location spanning 1 distinct geographic area - top geographies include 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.
-
Pain Relief After Trapeziectomy: Ibuprofen & Acetaminophen Versus Oxycodone
RECRUITING · Phase 2
-
Evaluation of Pain Management After Surgery When Using Exparel in the Pediatric Population
RECRUITING · Phase 2
-
Gabapentin to Reduce Opioid Use Postoperatively (GROUP) in Children
RECRUITING · Phase 2
-
Pectoral Nerve Blocks (PECs) for Cardiovascular Implantable Electronic Device Placement
ACTIVE NOT RECRUITING · Phase 2
-
Intraoperative Liposomal Bupivacaine vs. Bupivacaine for Total Hip Replacement Pain Management
COMPLETED · Phase 2
-
Perioperative Pregabalin in Ureteroscopy
COMPLETED · Phase 2
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
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.