Dexmedetomidine as an Adjunct to Periarticular Ropivacaine in Total Knee Replacement: A Pilot Randomised Controlled Trial

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-100
SponsorUniversity of Malaya

About this trial

This study aims to evaluate whether adding dexmedetomidine to ropivacaine-based periarticular infiltration (PAI) improves postoperative pain control in patients undergoing total knee replacement (TKR). Despite standard pain management, many patients continue to experience moderate-to-severe pain after surgery. Dexmedetomidine, a sedative and analgesic agent, may help prolong the effect of local anaesthetics. A total of 60 patients will be randomly assigned to receive either ropivacaine alone or ropivacaine with dexmedetomidine. Pain scores, opioid use, side effects, and recovery time will be monitored for 24 hours. The goal is to determine if this method is more effective and safer for improving recovery after knee surgery.

Eligibility criteria

Qualifiers

Aged ≥18 years

Undergoing elective unilateral total knee replacement

ASA physical status I-III

No known allergy to local anaesthetics or dexmedetomidine

Disqualifiers

Known allergy to study drugs

Chronic pain or neurological conditions

Bilateral or revision TKR

Significant deformity affecting function

Trial design

Treatments tested in this trial

  • Ropivacaine + saline solution
  • Ropivacaine + Dexmedetomidine

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators