Overview

Pain Relief by Intra-Peritoneal Nebulization of Ropivacaine Under Remifentanil Anesthesia for Gynecological Laparoscopy

Status:
Completed
Trial end date:
2010-10-01
Target enrollment:
0
Participant gender:
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 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Carmel Medical Center
Treatments:
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