Clinical Trials Directory

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

TypeNameDescription
DRUGNalbuphinepatient controlled analgesia with Nalbuphine
DRUGMorphinepatient 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.