Effects of Naloxane on Pain Control in Post operative Management of Hysterectomy Surgery
Not Applicable
- Conditions
- Pain.acute pain
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
1-ASA physical status I and II
scheduled for total abdominal hysterectomy with standadized general aneshteshia/
2-Age between 35-65 years old
Exclusion criteria :
1-Hepatic or Renal failure, Heart diseases,
2- history of drug allergy, substance abuse (including opioids and benzodiazepines) ,
3-morbid obesity,
4-history of postoperative nausea and vomiting(PONV),history of motion sickness
5- smokers
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Morphine Consumption. Timepoint: 0 ,30 min,1hr, 2hr, 4hr, 8hr, 16hr, 20hr, 24hr after surgery. Method of measurement: Opioid registration by milligrams.;Pain Intensity. Timepoint: 0 ,30 min,1hr, 2hr, 4hr, 8hr, 16hr, 20hr, 24hr after surgery. Method of measurement: NRS( Numeric Rating Score).
- Secondary Outcome Measures
Name Time Method Duration of operation. Timepoint: during the operation. Method of measurement: operating chart.;Intraoperative Fluid received. Timepoint: during the operation. Method of measurement: Crystaloid Fluid registration chart.;Pruritus. Timepoint: 0 ,30 min,1hr, 2hr, 4hr, 8hr, 16hr, 20hr, 24hr after surgery. Method of measurement: Numeric Rating score (NRS).;Post operative Nausea and Vomiting. Timepoint: 0 ,30 min,1hr, 2hr, 4hr, 8hr, 16hr, 20hr, 24hr after surgery. Method of measurement: NRS (Numeric Rating score).