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NCT00836316 Clinical Trial

Levobupivacaine During Cholecystectomy

Pain Clinical Trial

Official title:
Effects of Intraperitoneal Levobupivacaine on Pain After Laparoscopic Cholecystectomy: A Prospective, Randomized, Double-Blinded Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00836316
Other study ID # LDC-2008
Secondary ID
Status Completed
Phase Phase 4
First received February 3, 2009
Last updated February 3, 2009

Study information
Verified date February 2009
Source Ege University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects of intraperitoneal administration of levobupivacaine on pain after laparoscopic cholecystectomy.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- cholelithiasis

- chronic cholecystitis

Exclusion Criteria:

- hypersensitivity to local anesthetics

- acute cholecystitis

- morbid obesity

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• levobupivacaine
intraperitoneal administration of levobupivacaine on pain after laparoscopic cholecystectomy

Locations
Country Name City State
Turkey Ege University School of Medicine Izmir

Sponsors (1)
Lead Sponsor Collaborator
Ege University

Country where clinical trial is conducted

Turkey, 

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