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NCT05705050
Aminophylline Infusion on Pain Intensity After Ureterocopic Lithotripsy
Conditions: Aminophylline, Pain, Ureterocopic Lithotripsy
Sex: All
Ages: 18 Years – 65 Years
Phase: NA
Enrollment: 50
Sponsor: Tanta University
Location: Egypt
Summary
This study will be conducted to evaluate the effect of intraoperative systemic aminophylline infusion on pain intensity in patients undergoing ureteroscopic lithotripsy surgeries with ureteric stent placement at the end of the procedure.
Eligibility Criteria
Inclusion Criteria:Aged between 18 to 50 yearsAmerican society of anesthesiology (ASA) physical status I - IIBody mass index (BMI) less than 30.0 kg/m2Scheduled for ureteroscopic lithotripsy surgery with D-J ureteric stent placement at the end of procedureUnder general anesthesia.Exclusion Criteria:Patients with central nervous system diseases, cardiovascular diseases, arrhythmias, cerebrovascular diseases, convulsions, renal impairment or hepatic dysfunction.Pregnancy or lactation.Patients with a history of allergy to aminophylline.Coffee consumption (more than 2 cups/day)Patients with opioid addiction or patients treated with B agonists, tranquilizers, or antidepressants.Short procedures less than 30 minutes or procedures not requiring D-J stent placement.
Source: ClinicalTrials.gov (NCT05705050). StuddyBuddy aggregates publicly available trial information.