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Evaluation efficacy and side effects of IV ibuprofen and IV acetaminophen in pain control after laparoscopic cholecystectomy.

Phase 3
Conditions
Cholecystit.
Cholecystit
Registration Number
IRCT20161024030479N2
Lead Sponsor
Ardabil University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
90
Inclusion Criteria

Patients candidate for laparoscopic cholecystectomy
Age 20 - 60 years old

Exclusion Criteria

1-Pregnancy
Have a history of asthma and other respiratory disease
Have a history of heart failure
Have a history of CRF or dialysis
Have a history of GI bleeding
HTN
Have a history of Anemia
Patients are taking warfarin
Patients are taking a combination of ACEI and furosemide
Tolerance or dependence to opioids
Allergy or hypersensitivity to ibuprofen, ASA, NSAIDs, or COX2 inhibitor
Age less than 20 years old and more than 60 years old

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of pain in the surgical site. Timepoint: 6, 12, 18 and 24 hours after surgery. Method of measurement: VAS system.
Secondary Outcome Measures
NameTimeMethod
ausea and vomiting. Timepoint: 6,12,18 and 24 hours after surgery. Method of measurement: N/V Score.;Shoulder pain. Timepoint: 6,12,18 and 24 hours after surgery. Method of measurement: VAS.;Sedation. Timepoint: 6,12,18 and 24 hours after surgery. Method of measurement: Ramsay score.
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