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
| Type | Name | Description |
|---|---|---|
| DRUG | Sufentanil (R30730, brand name Sufenta) | sufentanil 1ug/ml |
| DRUG | Sufentanil (R30730, brand name Sufenta) + Morphine | sufentanil 0.5ug/ml+morphine 0.25mg/ml |
| DRUG | Morphine | morphine 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.