Clinical Trials Directory

Trials / Completed

CompletedNCT01917045

Different Lipid Soluble Opioids for Gynecologic Laparoscopic Surgery Postoperative Patient-controlled Analgesia

Different Lipid Soluble Opioids for Gynecologic Laparoscopic Surgery Postoperative Patient-controlled Analgesia --- a Double Blind Randomized Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
180 (actual)
Sponsor
Peking University First Hospital · Academic / Other
Sex
Female
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The investigators noticed that Body Fat Ratio might have great influence on the efficacy of different lipid soluble anesthetics. The objective of this clinical trial was to compare the effect of that Body Fat Ratio on the efficacy of different lipid soluble anesthetics.

Detailed description

The objective of this clinical trial was to compare the effect of that Body Fat Ratio on the efficacy of different lipid soluble anesthetics.

Conditions

Interventions

TypeNameDescription
DRUGSufentanil (R30730, brand name Sufenta)sufentanil 1ug/ml
DRUGSufentanil (R30730, brand name Sufenta) + Morphinesufentanil 0.5ug/ml+morphine 0.25mg/ml
DRUGMorphinemorphine 0. 5mg/ml

Timeline

Start date
2012-01-01
Primary completion
2013-03-01
Completion
2013-03-01
First posted
2013-08-06
Last updated
2013-08-06

Source: ClinicalTrials.gov record NCT01917045. Inclusion in this directory is not an endorsement.