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Comparison of analgesic effect of intravenous paracetamol and fentanyl during colonoscopy

Not Applicable
Conditions
Acute Pain.
Acute pain
Registration Number
IRCT201311227752N5
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 20-70 years; ASA class = 3
Exclusion criteria: age <20 years or> 70 years; Heart disease (arrhythmias, Aortic Stenosis, Ischemic Heart Disease,Heart failure) ; liver disease (Child-Pugh classification C);kidney disease ; lack of patient cooperation;mental illness (major Depression, mania, psychosis); Hypotension;Hypertension; drug addiction.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: 12 hours after colonoscopy. Method of measurement: Visoal analoge Scale.
Secondary Outcome Measures
NameTimeMethod
Sedation. Timepoint: 12 hours after clonoscopy. Method of measurement: Ramsay Sedation Scale.;Nause and vomiting. Timepoint: 12 hours after clonoscopy. Method of measurement: yes/no.
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