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Analgesia Comparison of Nalbuphine and Morphine for Laparoscopic Myomectomy

Postoperative Pain Clinical Trial

Official title:
Analgesia Comparison of Nalbuphine and Morphine for Laparoscopic Myomectomy

Clinical Trial Summary

to compare the analgesia and side effect of nalbuphine and morphine for elective Laparoscopic myomectomy.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03288428
Study type Interventional
Source Peking University First Hospital
Contact Yan Zhou, MD
Phone 13641202040
Email zhouyanlion@163.com
Status Recruiting
Phase Phase 4
Start date May 1, 2017
Completion date December 31, 2018
View Details
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