Status:
COMPLETED
Pain After Laparoscopic Cholecystectomy
Lead Sponsor:
Baylor College of Medicine
Conditions:
Postoperative Pain
Eligibility:
All Genders
18-64 years
Phase:
NA
Brief 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 laparoscopi...
Eligibility Criteria
Inclusion
- Patient ages 18-64
- American Society of Anesthesiology Physical Status I, II or III
- Inpatients scheduled to undergo laparoscopic cholecystectomy at Ben Taub General Hospital
Exclusion
- Open cholecystectomy - excluded due to increased levels of pain in open procedures
- Scheduled for ambulatory surgery
- Renal dysfunction (Serum Cr \> 1.2) - excluded due to potential altered metabolism of anesthetic and pain medications
- Allergy to any of the study medications or anesthetic agents
- Chronic opioid analgesic use at home - excluded due to potential difficulty in assessing pain caused by the procedure alone
- Patient inability to properly describe postoperative pain to investigators (language barrier, dementia, delirium, psychiatric disorder)
- Patient or surgeon refusal
Key Trial Info
Start Date :
September 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2010
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT00983918
Start Date
September 1 2009
End Date
June 1 2010
Last Update
February 1 2019
Active Locations (1)
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1
Ben Taub General Hospital
Houston, Texas, United States, 77030