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OpenTrials
Completed

NCT Number: NCT06357013

Postoperative Analgesia in Bilateral Knee Arthroplasties

To observationally compare the analgesic efficacy of LIA and S-FICB techniques and to record the pain scores of patients who underwent bilateral knee operations in the postoperative period.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Planned elective bilateral knee arthroplasty under spinal anesthesia
  • American Society of Anesthesiologists (ASA) risk score I-II
  • Patients aged 18-75 years

Exclusion criteria

  • Those receiving general anesthesia,
  • Those with epidural catheters,
  • Those who refused to participate in the study,
  • Those whose spinal anesthesia failed and returned to general anesthesia,
  • Those with a body mass index (BMI) >30 kg/m2,
  • History of chronic opioid or corticosteroid use,
  • Patients with psychiatric or neurological problems that would not allow assessment of pain using a visual analog scale (VAS) will be excluded.
  • In addition, patients whose surgery lasted <40 minutes or >120 minutes will also be excluded to keep the data homogeneous.

Treatment and study plan

Bilateral Suprainguinal fascia iliaca compartment block

Procedure

Suprainguinal fascia iliaca compartment block (S-FICB) is one of the commonly used regional analgesia techniques for postoperative analgesia in lower extremity surgeries.

Local Infiltration Analgesia

Procedure

Local infiltration analgesia is applied to the posterior part of the knee, including the periosteum, ligaments, muscle and/or skin area before closing the surgical field.

Primary outcomes

  1. Suprainguinal fascia iliaca compartment block (S-FICB) produces adequate analgesic effect in knee arthroplasty.

    Time frame: 4 months

    The aim of this study was to observationally compare the analgesic efficacy of local infiltration analgesia (LIA) and suprainguinal fascia iliaca compartment block (S-FICB) techniques in patients who underwent bilateral knee operations. Postoperative pain follow-up of the patients will be done by recording Visual analog scales (VAS) at 4, 8, 12 and 24 hours. Additional analgesic needs and unwanted side effects will also be recorded.

Sponsors and collaborators

Lead sponsor

Kocaeli City Hospital

Other Gov

Registry information

Official study title

Postoperative Analgesia in Bilateral Knee Arthroplasties:Suprainguinal Fascia Iliaca Compartment Block and Local Infiltration Analgesia

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Apr 10, 2024
Registry last updated
Jan 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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