Comparison of Sublingual buprenorphine and intravenous morphine for postoperative analgesic effect hemodynamic changes, nausea & vomiting

Not Applicable

• Conditions: Spinal anesthesia in ASA ClassI, II.; Other complications of anaesthesia; Other comp

• Registration Number: IRCT201012203305N2
• Lead Sponsor: Vice-chancellor for Research, Babol University Of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Age 18-60 years old, ASA Class I, II, candidate for lower limbs orthopedic surgery, herniorraphy, or varicocelectomy
Exclusion criteria: History of complications such as: respiratory, cardiovasculer diseases, hypertension, diabetes mellitus, or addiction

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative analgesic effect. Timepoint: before intervention untill 12 hours after intervention. Method of measurement: Visual analogue pain score.;Hemodynamic changes. Timepoint: before intervention untill 12 hours after intervention. Method of measurement: Pulse Oxymeter , Sphigmo manometer.;Nausea & Vomiting. Timepoint: Before intervention untill 12 hour after intervention. Method of measurement: Visual - questional.

Secondary Outcome Measures

Name	Time	Method
Oxygen saturation. Timepoint: 15, 30, 60 min after procedure, half an hour, before and after 2 and 12 hours. Method of measurement: pulse oximeter.