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Comparison of analgesic and sedative effect of combined propofol plus fentanyl and propofol plus ketamine

Not Applicable
Conditions
Sedation.
Other and unspecified general anaesthetics
Registration Number
IRCT201410187752N6
Lead Sponsor
Vice-chancellor of research of Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

age 18-80 years; ASA class = 3 Exclusion criteria: age <18 years or> 80 years; Heart disease (arrhythmias, Aortic Stenosis, Ischemic Heart Disease,Heart failure) ; liver disease (Child-Pugh classification C); drug addiction.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sedation. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: Ramsay Sedation Scale.;Pain. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: Visual Analoge Scale.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: sphygmomanometer.;Respiratory Rate. Timepoint: Every 2 minutes till 10 minutes and then every 5 minutes till 1 houre. Method of measurement: observation.
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