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Postoperative Analgesia in Bilateral Knee Arthroplasties

K

Kocaeli City Hospital

Status

Completed

Conditions

Peripheral Nerve Block
Knee Arthroplasty, Total
Pain, Postoperative

Treatments

Procedure: Bilateral Suprainguinal fascia iliaca compartment block
Procedure: Local infiltration analgesia

Study type

Observational

Funder types

Other

Identifiers

NCT06357013
2023-40

Details and patient eligibility

About

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.

Enrollment

40 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

40 participants in 2 patient groups

Grup-1: Suprainguinal fascia iliaca compartment block
Treatment:
Procedure: Bilateral Suprainguinal fascia iliaca compartment block
Grup-2: Local infiltration analgesia
Treatment:
Procedure: Local infiltration analgesia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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