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Intravenous Tramadol Versus Intravenous Paracetamol in Patients With Dysmenorrhea

Dysmenorrhea Clinical Trial

Official title:
Efficacy and Safety of Intravenous Tramadol Versus Intravenous Paracetamol for Relief of Acute Pain of Primary Dysmenorrhea: A Randomized Controlled Trial

Clinical Trial Summary

Patients presented with primary dysmenorrhea composed the study population. One gram paracetamol and 100 mg tramadol in 100 ml saline with a slow infusion were compared in ceasing dysmenorrhea in the emergency department

Clinical Trial Description

Patients over 18 years old who presented with dysmenorrhea composed the study population. Patients received painkiller within the last six hours, physical findings consistent with peritoneal irritation, allergy to the study drugs, renal or liver failure, drug addiction, pregnancy or woman with lactation and denied to give inform consent were the exclusion criteria. The pain of the study patients is measured with the visual analogue scale at baseline, 15th and 30th minutes and 1 hour after study drug administration. At the end of the 60 minutes, rescue drug need is also recorded. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03509740
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase Phase 4
Start date April 25, 2018
Completion date October 20, 2018
View Details
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