Postoperative Pain and Analgesic Use After Total Knee Arthroplasty

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorTomas Bata Hospital, Czech Republic

About this trial

This prospective observational study evaluates postoperative pain intensity and analgesic consumption in patients undergoing total knee arthroplasty (TKA) under different anesthesia techniques. Patients receive either general anesthesia with peripheral nerve block, spinal anesthesia with peripheral nerve block, spinal anesthesia alone, or general anesthesia with an epidural catheter. Pain scores (NRS), analgesic use, adverse effects, patient satisfaction, and the need for therapeutic interventions are assessed during the first 48 hours after surgery. The study aims to identify differences in postoperative pain control and factors associated with hypotension and other complications.

Eligibility criteria

Qualifiers

Age 18-100 years

Primary total knee arthroplasty (TKA)

ASA physical status I-III

Glasgow Coma Scale (GCS) score of 15

Disqualifiers

Revision or reoperation of TKA

ASA score IV or higher

Refusal to participate or inability to provide informed consent

GCS ≤ 14

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

50 Participants
are grouped into 4 trial groups