Periarticular Injection Versus Fascia Iliaca Block for Total Knee Arthroplasty

NCT ID: NCT02047331

Last Updated: 2014-01-28

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

66 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-02-28

Study Completion Date

2013-08-31

Brief Summary

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In this study, the aim is to compare the efficacy of Periarticular multimodal drug injection(group PI) and Fascia Iliaca Compartment Block ( group FI)for total knee arthroplasty.

Detailed Description

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Total knee arthroplasty is very painful surgical intervention.Patients were assigned to 2 groups to receive either periarticular multimodal drug injection or fascia iliaca compartment block for postoperative pain.

Conditions

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Total Knee Arthroplasty

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors

Study Groups

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group PI

group PI were performed periarticular drug injection during surgery.

Group Type ACTIVE_COMPARATOR

periarticular injection

Intervention Type PROCEDURE

patients were performed bupivacaine solution to the periarticular soft tissues during surgery by the surgeon.

group FI

group FI were performed fascia iliaca block before surgery

Group Type ACTIVE_COMPARATOR

fascia iliaca block

Intervention Type PROCEDURE

patients were performed fascia iliaca block with bupivacaine solution before surgery.

Interventions

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periarticular injection

patients were performed bupivacaine solution to the periarticular soft tissues during surgery by the surgeon.

Intervention Type PROCEDURE

fascia iliaca block

patients were performed fascia iliaca block with bupivacaine solution before surgery.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patients undergoing knee arthroplasty
* \> 18 years of age

Exclusion Criteria

* obesity
* heart failure
* kidney failure
* liver failure
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Baskent University

OTHER

Sponsor Role lead

Responsible Party

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CAGLA BALI,MD

MD,Anesthesiology and Reanimation

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Anis Aribogan, Prof.,MD

Role: STUDY_DIRECTOR

Baskent University School of Medicine

Locations

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Baskent University School of Medicine Adana Teaching and reserach Hospital

Adana, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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KA12/269

Identifier Type: -

Identifier Source: org_study_id

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