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Clinical Trials/NCT06196359
NCT06196359
Completed
Not Applicable

Assessing Function and Pain After Total Knee Arthroplasty With Combined Femoral and Popliteal Nerve Block

University of Haifa1 site in 1 country34 target enrollmentNovember 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Arthroplasty
Sponsor
University of Haifa
Enrollment
34
Locations
1
Primary Endpoint
Numeric Pain Rating Scale
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this interventional study is to examine whether a pain management technique of combined femoral and popliteal nerve block is effective in total knee arthroplasty patients. The main questions it aims to answer are:

Are there differences in postoperative outcomes? Does the nerve block, age, preoperative quadriceps muscle strength and Oxford Knee Score of the patient predict early functional ability? Participants underwent total knee arthroplasty and assessments. Researchers compared pain management techniques to assess effects on postoperative outcomes and identified the importance of preoperative variables a predictors of early functional ability. Further research is required to refine postoperative pain management strategies.

Registry
clinicaltrials.gov
Start Date
November 1, 2022
End Date
August 14, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Over the age of 18
  • Electively assigned for primary knee replacement surgery.
  • The American Society of Anesthesiologists physical status score 1-3.

Exclusion Criteria

  • Revision surgery.
  • Patients suffering from chronic pain syndrome or chronic opioid use.
  • Patients with previous neurological deficits in the lower extremities.
  • A cognitive state that does not allow signing of consent or understanding simple instructions.

Outcomes

Primary Outcomes

Numeric Pain Rating Scale

Time Frame: up to four days after surgery

An 11-point scale scored from 0 to 10: 0 = no pain, 10= the most intense pain imaginable

Quadriceps Muscle Strength

Time Frame: A 1 day before the surgery, first day after the surgery and third or fourth day after the surgery .

muscle strength measure by dynamometer (N⋅m)

Timed up & go Test

Time Frame: First day after surgery and third or fourth day after surgery

Total time to arise from chair, walk 3 m, turn around, return to chair and sit down. Two trials performed and the faster of the two is recorded to the nearest 10th of a second.

Secondary Outcomes

  • Surgery Duration(During the surgery)
  • Occurrence of Falls(At discharge (assessed up to day 10))
  • Elderly Mobility Scale(First day after the surgery and third or fourth day after the surgery)
  • Consumption of Analgesics(At discharge (assessed up to day 10))
  • 5 Times Sit to Stand Test(First day after the surgery and third or fourth day after the surgery)
  • Hospitalization Duration(At discharge (assessed up to day 10))
  • Oxford Knee Score Questionnaire(A 1 day before the surgery)

Study Sites (1)

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