Status:
COMPLETED
Pain Relief by Intra-Peritoneal Nebulization of Ropivacaine Under Remifentanil Anesthesia for Gynecological Laparoscopy
Lead Sponsor:
Carmel Medical Center
Conditions:
Gynecological Laparoscopy
Eligibility:
FEMALE
18-80 years
Phase:
PHASE3
Brief Summary
In our prospective, randomized, placebo controlled and double-blinded study we will study the efficacy of intraperitoneal ropivacaine nebulization on pain relief during gynecologic laparoscopic surger...
Detailed Description
Outcome Measures : * VAS score * Use of analgesics during operation and postoperative period
Eligibility Criteria
Inclusion
- Elective gynecological laparoscopic surgery including unilateral or bilateral salpingo-oophorectomy or ovarian cystectomy
- Patient not participating in other medical study at present or during the last 30 days
- Patient is capable of reading, understanding and signing on an informed consent
- Age 18 years and above
- ASA physical status grade 1-2
Exclusion
- Allergy to ropivacaine or other local anesthetics or other medications listed in the protocol
- Acute pelvic inflammatory disease
- Coumadin or aspirin treatment
- Significant arrythmias
- Analgesic treatment for chronic pain
- BMI\>35
Key Trial Info
Start Date :
June 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2010
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT00927979
Start Date
June 1 2009
End Date
October 1 2010
Last Update
June 28 2011
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