Trials / Completed
CompletedNCT03173339
Influence of Remifentanil on Postoperative Sore Throat in Patients Undergoing General Anesthesia
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 92 (actual)
- Sponsor
- Keimyung University Dongsan Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This investigation is planned to compare the incidence and severity of postoperative sore throat according to the dose of remifentanil.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Endotracheal intubation using laryngoscope | Endotracheal intubation was done using laryngoscope for general anesthesia. |
| DRUG | High remifentanil | Remifentanil was started as 0.25 mcg/kg/min. Remifentanil dose was adjusted to maintain blood pressure (20% of preoperative blood pressure) and bispectral index (40-60) by 0.05 mcg/kg/min. |
| DRUG | Low remifentanil | Remifentanil was administered as 0.1 mcg/kg/min. |
| DRUG | High sevoflurane | Sevoflurane was started as 0.5 MAC. Sevoflurane dose was adjusted to maintain blood pressure (20% of preoperative blood pressure) and bispectral index (40-60) by 0.2 %. |
| DRUG | Low sevoflurane | Sevoflurane was administered as 0.5 MAC. |
Timeline
- Start date
- 2017-06-01
- Primary completion
- 2017-08-24
- Completion
- 2017-08-24
- First posted
- 2017-06-01
- Last updated
- 2017-08-25
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03173339. Inclusion in this directory is not an endorsement.