Trials / Unknown
UnknownNCT03288428
Analgesia Comparison of Nalbuphine and Morphine for Laparoscopic Myomectomy
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Peking University First Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
to compare the analgesia and side effect of nalbuphine and morphine for elective Laparoscopic myomectomy.
Detailed description
To compare the analgesia and side effect of nalbuphine and morphine for elective Laparoscopic myomectomy, by using patient controlled analgesia postoperatively, a randomized, double blind clinical trial. Patients undergoing elective Laparoscopic myomectomy are randomly divided into two groups: nalbuphine and morphine groups. All patients are under general anesthesia with routine methods. The nalbuphine group receive postoperative patient controlled analgesia using nalbuphine 30mg/120ml, while the morphine group receive postoperative patient controlled analgesia using morphine 60mg/120ml. Perioperative parameters are to be collected to compare the two groups.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nalbuphine | patient controlled analgesia with Nalbuphine |
| DRUG | Morphine | patient controlled analgesia with Morphine |
Timeline
- Start date
- 2017-05-01
- Primary completion
- 2018-12-31
- Completion
- 2018-12-31
- First posted
- 2017-09-20
- Last updated
- 2017-11-06
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03288428. Inclusion in this directory is not an endorsement.