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The effect and comparison of oral and intravenous Acetaminophen in pain cardiac surgery patients

Phase 2
Conditions
Coronary and valvular heart surgery.
Other functional disturbances following cardiac surgery
Registration Number
IRCT2016022026217N2
Lead Sponsor
Vice Chancellor for research, Lorestan University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
160
Inclusion Criteria

all patients who underwent CABG surgery with or without valve replacement; age older than 18 or less than 65 years; absence of addiction to drugs or alcohol; absence of allergy or hypersensitivity to acetaminophen or narcotics; absence of impaired kidney function (creatinine level Less than 2 milligrams per deciliter); no history of liver failure; no history of sleep apnea. Exclusion criteria: Visual analog scale score is higher than 7 after extubation; not wanting to continue cooperation?; use of narcotic drugs and sedatives during the procedure?; decreased level of consciousness of the patient during the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Amount of pain. Timepoint: Minute 0, 20, 80 and 120 after receiving the first dose. Method of measurement: visual analog scale.;The amount of narcotic. Timepoint: 24 hours after receiving the first dose. Method of measurement: Milligrams per kilogram of body weight.
Secondary Outcome Measures
NameTimeMethod
The best pattern of use drug on regular basis or on when necessary. Timepoint: 24 hours after receiving the first dose. Method of measurement: Visual anlog scale and milligrams per kilogram of body weight.;Nausea. Timepoint: frequency during the first 24 hours after receiving the first dose. Method of measurement: history taking from patient or nurses.;Vomiting. Timepoint: frequency during the first 24 hours after receiving the first dose. Method of measurement: history taking from patient or nurses.;Need for antiemetics. Timepoint: frequency during the first 24 hours after receiving the first dose. Method of measurement: information taken from patient's records.
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