Trials / Completed
CompletedNCT03147066
Dezocine for Prevention of Catheter-related Bladder Discomfort
Efficacy of Dezocine for the Prevention of Catheter-related Bladder Discomfort
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 96 (actual)
- Sponsor
- Jian-jun Yang · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This study evaluates the efficacy of dezocine in preventing the catheter-related bladder discomfort (CRBD) in a postanesthesia care unit (PACU).
Detailed description
Thirty min before the end of the surgery, patients were randomly assigned to one of the two group to receive intravenous dezocine 0.1 mg/kg (Group D, n=48) or flurbiprofen axetil 1 mg/kg (Group F, n=48) . The CRBD was assessed at 0, 1, 2, and 6 h after patient's arrival in the post-anaesthesia care unit. Severity of CRBD was graded as none, mild, moderate and severe.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dezocine | Dezocine (0.1 mg/kg)will be infused during surgery |
| DRUG | Flurbiprofen Axetil | Flurbiprofen Axetil (1 mg/kg)will be infused during surgery |
Timeline
- Start date
- 2017-09-01
- Primary completion
- 2017-10-30
- Completion
- 2017-10-30
- First posted
- 2017-05-10
- Last updated
- 2017-10-31
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03147066. Inclusion in this directory is not an endorsement.