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Clinical Trials/NCT05636449
NCT05636449
Completed
Not Applicable

Ultrasound Guided Suprainguinal Fascia Iliaca Block vs. Periarticular Injection for Total Knee Arthroplasty: Prospective Randomized Study

Ataturk University1 site in 1 country70 target enrollmentNovember 25, 2022
ConditionsAnalgesia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Analgesia
Sponsor
Ataturk University
Enrollment
70
Locations
1
Primary Endpoint
Postoperative opioid consumption
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Total knee replacement (total knee arthroplasty) is performed to resurface a knee damaged by arthritis and relieve pain in patients with severely damaged knee joints.

Total knee arthroplasty (TKA) is associated with severe postoperative pain, and the management of postoperative pain continues to evolve with the advancement of surgical techniques and pharmacological treatments.

Femoral, lateral femoral cutaneous nerve and obturator nerve block is provided with suprainguinal fascia iliaca plan block, which is used for postoperative analgesia, especially in hip surgeries. In this way, the investigators think it can be used as a part of multimodal analgesia in total knee arthroplasty surgery.

Registry
clinicaltrials.gov
Start Date
November 25, 2022
End Date
May 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Elif Oral Ahiskalioglu

Principal Investigator

Ataturk University

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologist's physiologic state I-III patients
  • Total knee arthroplasty

Exclusion Criteria

  • liver, kidney, and advanced heart failure,
  • routine use of analgesics and
  • having used analgesics in the last 24 hours,
  • having neuropathic pain,
  • refusal to participate in the study

Outcomes

Primary Outcomes

Postoperative opioid consumption

Time Frame: first 24 hours

First 24 hours total fentanyl consumption with patient controlled analgesia

Secondary Outcomes

  • joint range of motion test (ROM)(at 24th hour)
  • Visual analog pain score(first 48 hours)
  • Five Time Sit to Stand Test (FTSST)(at 24th hour)
  • timed up and go test (TUG)(at 24th hour)
  • quadriceps muscle strength(at 24th hour)

Study Sites (1)

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