Trials / Unknown
UnknownNCT02674737
Evaluation of the Effect of Appropriate Sedation for Patients After Gastrectomy: A Prospective Randomised Controlled Study
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Chinese Medical Association · Network
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the efficacy and safety of appropriate postoperative sedation with dexmedetomidine for patients after gastrectomy. Prospective randomised controlled study was conducted from October 2015 and December 2015 among patients after gastrectomy. The investigators are going to enroll patients who received abdominal surgeries. One group receive sedative along with analgesic and the other group analgesic only for the other group on the first 24 hours after surgeries and follow up for 3 days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | dexmedetomidine, tramadol and flurbiprofen | |
| DRUG | tramadol and flurbiprofen |
Timeline
- Start date
- 2016-01-01
- Primary completion
- 2016-05-01
- First posted
- 2016-02-04
- Last updated
- 2016-02-04
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02674737. Inclusion in this directory is not an endorsement.