Clinical Trials Directory

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

TypeNameDescription
DRUGDezocineDezocine (0.1 mg/kg)will be infused during surgery
DRUGFlurbiprofen AxetilFlurbiprofen 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.