Overview
Pain Relief by Intra-Peritoneal Nebulization of Ropivacaine Under Remifentanil Anesthesia for Gynecological Laparoscopy
Status:
Completed
Completed
Trial end date:
2010-10-01
2010-10-01
Target enrollment:
0
0
Participant gender:
Female
Female
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 surgery. This is a second steady with protocol of general anesthesia used of Remifentanil.Phase:
Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Carmel Medical CenterTreatments:
Remifentanil
Ropivacaine
Criteria
Inclusion Criteria:- 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 Criteria:
- 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