CI

At a glance

ClinicalIndex Comparison Record
Phase 4Terminated· 3 enrolled
Drug / intervention
Dexmedetomidine +1 moredrug
Likely dose
Dexmedetomidine 250mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03629483
NCT03629483Phase 4Terminated
Terminated

Impact of Dexmedetomidine Combined With Ropivacaine for Postoperative Continuous Femoral Nerve Block on Postoperative Delirium and Long-term Oucomes in Elderly Patients After Single Knee Arthroplasty

Peking University First Hospital·interventional·Posted Aug 14, 2018·Updated Aug 3, 2025

In Brief

A Phase 4 clinical trial evaluating Dexmedetomidine and Placebo for Elderly and 5 related conditions. Terminated early, enrolled 3 participants.

Signals

Trial was terminated early

Detailed Summary

Delirium is common in the elderly after orthopedic surgery and is associated with worse outcomes. Continuous femoral nerve block is frequently used for postoperative analgesia after total knee arthoplasty. The investigators hypothesize that dexmedetomidine, when combined with ropivacaine for continuous femoral nerve block, can reduce the incidence of delirium and improve the long-term outcome in elderly patients after total knee arthroplasty.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--

Timeline

Phase 4TerminatedFinished
20192020202120222023202420252026
First PostedAug 14, 2018
Enrollment StartDec 10, 2018
Primary CompletionDec 14, 2018
TodayJul 1, 2026
Enrollment to primary: 4 daysPosted 7.9 years ago

Interventions

Dexmedetomidinedrug

Patients in this group receive continuous femoral nerve block analgesia for 48 hours after surgery. The formula is a mixture of 0.2% ropivacaine 250ml and 3.75 ug/kg dexmedetomidine. The analgesic pump is set to administer a continuous infusion at a rate of 5 ml/h (equivalent to a dexmedetomidine infusion at a rate of 0.075 ug/kg/h).

Placebodrug

Patients in this group receive continuous femoral nerve block analgesia for 48 hours after surgery. The formula is a mixture of 0.2% ropivacaine 250 ml and placebo. The analgesic pump is set to administer a continuous infusion at a rate of 5 ml/h.