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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