Levobupivacaine During Cholecystectomy

NCT ID: NCT00836316

Last Updated: 2009-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Brief Summary

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

Detailed Description

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Conditions

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Cholelithiasis Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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levobupivacaine

intraperitoneal administration of levobupivacaine on pain after laparoscopic cholecystectomy

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* cholelithiasis
* chronic cholecystitis

Exclusion Criteria

* hypersensitivity to local anesthetics
* acute cholecystitis
* morbid obesity
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ege University

OTHER

Sponsor Role lead

Locations

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Ege University School of Medicine

Izmir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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LDC-2008

Identifier Type: -

Identifier Source: org_study_id

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