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
| Type | Name | Description |
|---|---|---|
| DRUG | Sufentanil | The infusion rate of sufentanil is adjusted to achieve a surgical pleth index of 20-50 throughout the operative time. |
| DRUG | Remifentanil | The 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.