Trials / Completed
CompletedNCT02146976
Postoperative Sleep Quality of Patients Anesthesia With Propofol or Sevoflurane Undergoing Thyroidectomy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 124 (actual)
- Sponsor
- China Medical University, China · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The investigators designed a study to determine whether Propofol or Sevoflurane would provide same postoperative sleep quality in patients undergoing thyroidectomy.
Detailed description
The investigators designed a study to determine whether Propofol or Sevoflurane would provide same postoperative sleep quality in patients undergoing thyroidectomy.The bispectral index score (BIS) was monitored during the operation and the first postoperative night.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | propofol | introvenious infusion of propofol |
| DRUG | sevoflurane | sevoflurane (1.0-1.3 Minimum Alveolar Concentration) |
Timeline
- Start date
- 2014-10-01
- Primary completion
- 2015-09-01
- Completion
- 2015-10-01
- First posted
- 2014-05-26
- Last updated
- 2016-01-29
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02146976. Inclusion in this directory is not an endorsement.