CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,500 enrolled
Drug / intervention
Dexmedetomidine supplemented morphine analgesia +1 moredrug
Likely dose
Dexmedetomidine supplemented morphine analgesia 0.5 mgfrom 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/NCT03012971
NCT03012971N/ACompleted

Impact of Dexmedetomidine Supplemented Analgesia on Long-term Survival in Elderly Patients After Cancer Surgery: a Multicenter Randomized Controlled Trial

Peking University First Hospital·interventional·Posted Jan 6, 2017·Updated Jan 8, 2026

In Brief

A clinical study evaluating Dexmedetomidine supplemented morphine analgesia and Morphine analgesia for Elderly and 4 related conditions. Completed, enrolled 1,500 participants across 12 sites.

Detailed Summary

A majority of the elderly patients undergo surgery for malignant tumors. For these patients, postoperative tumor recurrence and metastasis are main factors that worsen long-term outcomes. The investigators hypothesize that dexmedetomidine supplemented analgesia in elderly patients after cancer surgery may help to maintain immune function and improve long-term outcomes, possibly by relieving stress and inflammatory response, improving analgesic efficacy and sleep quality, and reducing delirium incidence.

Study Details

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJan 6, 2017
Enrollment StartJan 6, 2017
Primary CompletionDec 11, 2024
TodayJul 1, 2026
Enrollment to primary: 7.9 yearsPosted 9.5 years ago

Interventions

Dexmedetomidine supplemented morphine analgesiadrug

Patients in this group receive patient-controlled intravenous analgesia for 3 days after surgery. The formula is a mixture of dexmedetomidine (1.25 ug/ml) and morphine (0.5 mg/ml), diluted with normal saline to 160 ml. 5-HT3 receptor antagonist is added when necessary. The analgesic pump is set to administer a background infusion at a rate of 1 ml/h, with a bolus dose of 2 ml at each time and a lockout time from 6 to 8 minutes.

Morphine analgesiadrug

Patients in this group receive patient-controlled intravenous analgesia for 3 days after surgery. The formula is morphine (0.5 mg/ml), diluted with normal saline to 160 ml. 5-HT3 receptor antagonist is added when necessary. The analgesic pump is set to administer a background infusion at a rate of 1 ml/h, with a bolus dose of 2 ml at each time and a lockout time from 6 to 8 minutes.