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Ultrasound Guided Transversus Abdominis Plane (TAP) Block for Postoperative Analgesia After Laparoscopic Colonic Resection

NCT ID: NCT01423292

Last Updated: 2012-08-06

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

PHASE3

Total Enrollment

56 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-08-31

Study Completion Date

2012-04-30

Brief Summary

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The purpose of this study is to determine whether the transversus abdominis plane (TAP) blocks are effective in postoperative pain control of adult patients undergoing laparoscopic colectomy.

Detailed Description

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Conditions

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Laparoscopic Colecctomy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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an odd numbered patients

TAP block with local anesthetics

Group Type ACTIVE_COMPARATOR

Ultrasound Guided Transversus Abdominis Plane (TAP) Block

Intervention Type PROCEDURE

Ultrasound Guided Transversus Abdominis Plane (TAP) Block

bupivacaine

Intervention Type DRUG

0.25 bupivacaine 30ml (15ml on each side)

an even numbered patients

TAP block without local anesthetics

Group Type PLACEBO_COMPARATOR

Ultrasound Guided Transversus Abdominis Plane (TAP) Block

Intervention Type PROCEDURE

Ultrasound Guided Transversus Abdominis Plane (TAP) Block

Placebo

Intervention Type DRUG

placebo

Interventions

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Ultrasound Guided Transversus Abdominis Plane (TAP) Block

Ultrasound Guided Transversus Abdominis Plane (TAP) Block

Intervention Type PROCEDURE

bupivacaine

0.25 bupivacaine 30ml (15ml on each side)

Intervention Type DRUG

Placebo

placebo

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* aged 20\~80
* undergoing laparoscopic colectomy

Exclusion Criteria

* allergic history to local anesthesitcs
* tolerance to opioid
* cannot use IV-PCA
* previous abdominal surgery
* intestinal obstruction
* emergency
Minimum Eligible Age

20 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Center, Korea

OTHER_GOV

Sponsor Role lead

Responsible Party

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Ji Won Park

Center for Colorectal Cancer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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National Cancer Center

Goyang-si, Gyeonggi-do, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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NCCCTS-11-557

Identifier Type: -

Identifier Source: org_study_id