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NCT00983918 · ClinicalTrials.gov registry record · NA
Pain After Laparoscopic Cholecystectomy
A NA study, sponsored by Baylor College of Medicine.
- Completed
- Registry status
- NA
- Development phase
- 80
- Enrollment target
NCT00983918 is a NA study that has completed, run by Baylor College of Medicine. The registered enrollment target is 80 participants.
The verdict
NCT00983918, a NA study, has completed, sponsored by Baylor College of Medicine.
- COMPLETED
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
Study Summary
To the investigators' knowledge, no study has looked at differences in postoperative pain when comparing maintenance of anesthesia with isoflurane, desflurane, sevoflurane, and propofol in laparoscopic cholecystectomy. The investigators' hypothesis is that total intravenous anesthesia with propofol will lead to less postoperative pain in the first 24 hours after laparoscopic cholecystectomy when compared to maintenance of anesthesia with isoflurane, desflurane or sevoflurane. PURPOSE To find out if maintenance of anesthesia with propofol leads to less postoperative pain after laparoscopic cholecystectomy when compared to maintenance of anesthesia with isoflurane, desflurane, or sevoflurane.
Interventions
- DRUG Sevoflurane
- DRUG Propofol
- DRUG Isoflurane
- DRUG Desflurane
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2009-09 |
| Est. Completion | 2010-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00983918
The ClinicalTrials.gov registry entry for NCT00983918 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Sevoflurane is the first listed.
NCT00983918 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00983918 about?
NCT00983918 is a clinical study titled "Pain After Laparoscopic Cholecystectomy". To the investigators' knowledge, no study has looked at differences in postoperative pain when comparing maintenance of anesthesia with isoflurane, desflurane, sevoflurane, and propofol in laparoscopic cholecystectomy. The investigators' hypothesis is that total intravenous anesthesia with propofol ...
What is the current status of trial NCT00983918?
This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2009-09. Estimated completion is 2010-06.
What interventions are being tested in trial NCT00983918?
The interventions under investigation include: Sevoflurane (DRUG), Propofol (DRUG), Isoflurane (DRUG), Desflurane (DRUG).
Who is sponsoring clinical trial NCT00983918?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
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