Evaluation of oral Clonidine effects on prevention of post-anesthesia shivering

Not Applicable

Completed

• Conditions: post-anesthesia shivering.

• Registration Number: IRCT138902083773N2
• Lead Sponsor: Tehran University of Medical Sciences and Health Services

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Age 16-80 years, A.S.A I-II, elective surgery,
Exclusion criteria: Hypotension (B.P. < 80 mmHg), hypertensive (B.P.> 140/95 mmHg), cardiac, renal or liver disease, addiction, previous clonidine usage, pregnancy

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Shivering. Timepoint: End of Anesthesia (Recovery room). Method of measurement: Crossley & Mahajan shivering score.

Secondary Outcome Measures

Name	Time	Method
Mean blood pressure. Timepoint: During operation. Method of measurement: sphygmomanometer.;SpO2. Timepoint: During operation. Method of measurement: Pulse oximtry.;Heart rate. Timepoint: During operation. Method of measurement: Cardiac monitoring.;Emergence from anesthesia. Timepoint: At the end of anesthesia. Method of measurement: Time (minute) emergence from anesthesia.