Interaction Between Nalbuphine and Morphine in PCA

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT00155233
Collaborator
(none)
200
1

Study Details

Study Description

Brief Summary

  1. Nalbuphine is opioid mu receptor antagonist and kappa receptor agonist

  2. This study was designed to investigate the interaction between nalbuphine and morphine

Condition or Disease Intervention/Treatment Phase
  • Drug: Nalbuphine and morphine
Phase 4

Detailed Description

  1. Nalbuphine is opioid mu receptor antagonist and kappa receptor agonist

  2. This study was designed to investigate the interaction between nalbuphine and morphine

  3. The analgesic effect and opioid-related side effects will be investigated

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double
Primary Purpose:
Treatment
Official Title:
Interaction Between Nalbuphine and Morphine in Postoperative PCA for Gynecologic Patients
Study Start Date :
Jan 1, 2005

Outcome Measures

Primary Outcome Measures

  1. analgesic effect []

Secondary Outcome Measures

  1. incidence of opioid-related side effects []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age 18-65 y/o

  2. Female patients of ASA physical status I to III

  3. Scheduled for elective abdominal hysterectomy, myomectomy, or excision of ovarian tumor

Exclusion Criteria:
  1. Patients with a definite diagnosis of chronic pain syndrome, psychiatric disorders, or drug abuse (include opioids, NSAIDs, sedatives, antidepressants)

  2. Intraoperative fentanyl use > 3 μg/kg

  3. Patients with definite diagnosis of esophageal reflux syndrome

  4. Use of sedatives, antiemetics, or antipruritics within 24 hours before operation

  5. Surgery > 4 hours or laparoscopy surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwan University Hospital Taipei Taiwan 100

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Principal Investigator: Wei-Zen Sun, MD, National Taiwan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00155233
Other Study ID Numbers:
  • 931002
First Posted:
Sep 12, 2005
Last Update Posted:
Nov 23, 2005
Last Verified:
Jun 1, 2005
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 23, 2005