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Periarticular Injection Versus Fascia Iliaca Block for Total Knee Arthroplasty

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ClinicalTrials.gov Identifier: NCT02047331
Recruitment Status : Completed
First Posted : January 28, 2014
Last Update Posted : January 28, 2014
Sponsor:
Information provided by (Responsible Party):
CAGLA BALI,MD, Baskent University

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Total Knee Arthroplasty Procedure: periarticular injection Procedure: fascia iliaca block Phase 4

Detailed Description:
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.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 66 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Care Provider, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Multimodal Periarticular Injection Versus Fascia Iliaca Compartment Block for Total Knee Arthroplasty
Study Start Date : February 2013
Actual Primary Completion Date : July 2013
Actual Study Completion Date : August 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Knee Replacement

Arm Intervention/treatment
Active Comparator: group PI
group PI were performed periarticular drug injection during surgery.
Procedure: periarticular injection
patients were performed bupivacaine solution to the periarticular soft tissues during surgery by the surgeon.

Active Comparator: group FI
group FI were performed fascia iliaca block before surgery
Procedure: fascia iliaca block
patients were performed fascia iliaca block with bupivacaine solution before surgery.




Primary Outcome Measures :
  1. Postoperative pain scores of periarticular injection and fascia block for total knee arthroplasty [ Time Frame: postoperative 24 hours ]
    Patients were assigned in two groups to perform either periarticular injection (group PI) and fascia block ( group FB). They were accessed by visual analog scale. The aim was to compare the efficacy and side effects of periarticular injection and fascia block.



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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • patients undergoing knee arthroplasty
  • > 18 years of age

Exclusion Criteria:

  • obesity
  • heart failure
  • kidney failure
  • liver failure

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02047331


Locations
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Turkey
Baskent University School of Medicine Adana Teaching and reserach Hospital
Adana, Turkey, 01250
Sponsors and Collaborators
Baskent University
Investigators
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Study Director: Anis Aribogan, Prof.,MD Baskent University School of Medicine

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Responsible Party: CAGLA BALI,MD, MD,Anesthesiology and Reanimation, Baskent University
ClinicalTrials.gov Identifier: NCT02047331     History of Changes
Other Study ID Numbers: KA12/269
First Posted: January 28, 2014    Key Record Dates
Last Update Posted: January 28, 2014
Last Verified: January 2014

Keywords provided by CAGLA BALI,MD, Baskent University:
periarticular drug injection
fascia iliaca block
knee arthroplasty