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NOT YET RECRUITING
NCT07176065
PHASE4

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

Sponsor: University of Malaya

View on ClinicalTrials.gov

Summary

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.

Official title: A Pilot Randomized Controlled Trial Assessing the Impact of Dexmedetomidine as an Adjunct to Periarticular Ropivacaine Infiltration on Postoperative Pain and Recovery in Patients Undergoing Total Knee Replacement

Key Details

Gender

All

Age Range

18 Years - 100 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-10

Completion Date

2028-12

Last Updated

2025-09-16

Healthy Volunteers

No

Interventions

DRUG

Ropivacaine + saline solution

0.5% ropivacaine (19 mL) + 1 mL normal saline administered intraoperatively via periarticular injection.

DRUG

Ropivacaine + Dexmedetomidine

0.5% ropivacaine (19 mL) + dexmedetomidine 100 µg in 1 mL administered intraoperatively via periarticular injection.

Locations (1)

Universiti Malaya Medical Centre

Kuala Lumpur, Kuala Lumpur, Malaysia