Status:
COMPLETED
Different Lipid Soluble Opioids for Gynecologic Laparoscopic Surgery Postoperative Patient-controlled Analgesia
Lead Sponsor:
Peking University First Hospital
Conditions:
Post Operative Pain Management
Eligibility:
FEMALE
20-50 years
Phase:
NA
Brief 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 ...
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.
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists grade I-II
- adults aged over 20 and below 50 years old,
- non-smoker,
- with normal hepatic and renal function.
Exclusion
- smoker ,
- any kind of mental disorder or
- history use of analgesics for more than 10 consecutive days,
- asthma; and
- those with digestion tract disorder who would get nausea or vomiting much more easily than normal people.
Key Trial Info
Start Date :
January 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2013
Estimated Enrollment :
180 Patients enrolled
Trial Details
Trial ID
NCT01917045
Start Date
January 1 2012
End Date
March 1 2013
Last Update
August 6 2013
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