drugset / Trial / NCT02116868

Pupillary Reflex Measurement to Guide Intraoperative Analgesia During Laparoscopic Surgery

NCT02116868 ↗

Completed 100 enrolled Central Hospital, Nancy, France
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether analgesia guided by pupillary reflex during laparoscopic surgery is effective in opioid sparing (intraoperative remifentanil and postoperative morphine).This is a prospective, randomized, controlled study performed in two centers.

Timeline

Start
2014-03
Primary completion
2018-03
Completion
2018-04

Outcome

Met primary endpoint

paper Intraoperative remifentanil consumption was lower in the PRD-guided group than in the control group: PMID 33913678 ↗

paper with a mean difference (95% confidence Interval, CI) of 0.048 (0.035 to 0.060) μg kg-1 min-1; P < 0.0001. PMID 33913678 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Esmolol Other / unclassified — —
Subject Nicardipine Small molecule — —
Subject Remifentanil Small molecule — —
Subject Urapidil Small molecule — —

Indications

No indication recorded.