Phase
Condition
N/ATreatment
Granisetron 1 Mg/mL Intravenous Solution
Normal saline
Clinical Study ID
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients who are scheduled to undergo elective LC.
Adults (males and/or females) between the ages of 18-70 years old.
Exclusion
Exclusion Criteria:
Chronic pain other than cholelithiasis.
Patients who received analgesics or sedatives 24 h before scheduled surgery.
Severe hepatic (Child Pugh Class B and C) and renal dysfunction (CrCl <30ml/min)
Previous allergic response to granisetron.
Pregnancy and lactation
Patients with communication problems, cognitive dysfunction, or psychologicaldisorders
Daily corticosteroid use
Study Design
Study Description
Connect with a study center
National Hepatology and Tropical Research Institute
Cairo, 11617
EgyptSite Not Available
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