Trials / Completed
CompletedNCT01125982
Postoperative Fatigue and Nausea Related to Choice of Anaesthetic Regimens
Postanaesthetic Outcome and Assessment of Fatigue in Day-surgery Laparoscopic Cholecystectomy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 130 (actual)
- Sponsor
- Sykehuset Telemark · Other Government
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to establish validated outcome measures for Postoperative Fatigue and Postoperative nausea, and to compare clinical impact of postanaesthetic symptoms during first week after Propofol or Desflurane based anaesthesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol | Continuous intravenous infusion at 3-6 µg/mL (Ce - Target Controlled Infusion) during anaesthesia to provide sleep. |
| DRUG | Desflurane | Continuous inhalation at 0.7-0.8 MAC (endtidal) during anaesthesia to provide sleep |
Timeline
- Start date
- 2010-06-01
- Primary completion
- 2013-07-01
- Completion
- 2013-07-01
- First posted
- 2010-05-19
- Last updated
- 2014-11-19
Locations
1 site across 1 country: Norway
Source: ClinicalTrials.gov record NCT01125982. Inclusion in this directory is not an endorsement.