Clinical Trials Directory

Trials / Completed

CompletedNCT03868111

Sufentanil as Adjuvant of Balanced Anesthesia

Comparison Between Sufentanil and Remifentanil as General Anesthetic Adjuvant

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Kangbuk Samsung Hospital · Academic / Other
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of the study was to compare the efficacy and safety between sufentanil and remifentanil as an adjuvant of balanced general anesthesia.

Detailed description

The investigators hypothesized that sufentanil would reduce postoperative pain than remifentanil without prolonging recovery times in minor laparoscopic surgery when administered equivalent antinociceptive doses during surgery. Intraoperative opioid administration for equivalent nociception-antinociception balance could be achieved via surgical pleth index (SPI)-guided analgesia. This study was designed to compare the efficacy and safety between sufentanil and remifentanil as an adjuvant of balanced anesthesia in patients undergoing laparoscopic cholecystectomy under SPI-guided opioid administration.

Conditions

Interventions

TypeNameDescription
DRUGSufentanilThe infusion rate of sufentanil is adjusted to achieve a surgical pleth index of 20-50 throughout the operative time.
DRUGRemifentanilThe infusion rate of remifentanil is adjusted to achieve a surgical pleth index of 20-50 throughout the operative time.

Timeline

Start date
2019-11-04
Primary completion
2020-01-12
Completion
2020-01-12
First posted
2019-03-08
Last updated
2020-06-04

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03868111. Inclusion in this directory is not an endorsement.