Trials / Completed
CompletedNCT02793986
Dexmedetomidine vs Propofol Sedation Reduces Postoperative Delirium in Patients Receiving Hip Arthroplasty.
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 296 (actual)
- Sponsor
- The First Affiliated Hospital of Anhui Medical University · Academic / Other
- Sex
- All
- Age
- 65 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
With blocks of lumbar and lumbar plexus, we can reduce the intravenous anesthetics usage. To offer an satisfied surgery process for patients, a proper sedation is necessary. So in this study, we want to investigate the influence of two different sedative drugs on outcomes of patients received hip replacement surgery .
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | propofol | For patients in Group P, the sedation was achieved with a target-controlled infusion (TCI) of propofol, and the effect site concentration was set to 0.8-1.0μg/ml. |
| DRUG | dexmedetomidine | For patients in Group D, the sedation was achieved with a bolus of dexmedetomidine at 1.0 μg/kg (over a period of 15 to 20 min) and followed by an infusion of dexmedetomidine at 0.2-0.7 μg/kg/h. The depth of sedation was considered enough when patient was unresponsive to voice. |
Timeline
- Start date
- 2015-08-01
- Primary completion
- 2017-06-29
- Completion
- 2017-06-29
- First posted
- 2016-06-08
- Last updated
- 2017-06-29
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02793986. Inclusion in this directory is not an endorsement.