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Paracetamol-Tramadol and Paracetamol-caffeine Versus Placebo in the Emergency Discharge Treatment of Renal Colic
Sponsor: University of Monastir
Summary
This is a prospective, randomized, single-blind study. Patients included in the study after successful treatment of the acute attack were randomized upon discharge from the Emergency Department into three groups: oral paracetamol-tramadol group, oral paracetamol-caffeine group and oral placebo group.
Key Details
Gender
All
Age Range
18 Years - 99 Years
Study Type
INTERVENTIONAL
Enrollment
1500
Start Date
2024-04-10
Completion Date
2025-11-30
Last Updated
2024-09-19
Healthy Volunteers
No
Conditions
Interventions
paracétamol tramadol
Each patient received 1 tablet \* 2/day synalvic (325 mg of paracetamol + 37.5 mg of tramadol) for 7 days
Paracétamol cafeine
Each patient received 1 tab \* 3/d stopalgic extra (65mgcaffeine+500mg paracetamol) for 7 days
Placebo
Each patient received 1 tab \* 3 / d of placebo (flour) every day for 7 days
Locations (1)
Semir Nouira
Monastir, Tunisia