Comparison of Oral Paracetamol and Zolmitriptan Efficacy in the Treatment of Acute Migraine in Emergency Department
Launched by PAMUKKALE UNIVERSITY · May 8, 2017
Trial Information
Current as of May 27, 2025
Completed
Keywords
ClinConnect Summary
* This is prospective, randomized, controlled research to compare the efficacy of these two drugs in emergancy department.
* The clinical trial was conducted in the ED of Pamukkale University Medical Faculty Hospital.
* Study personnel (emergency physicians and nurses) were trained before the study.
* When oral drugs (paracetamol, zolmitriptan was being recommended, an eligibility checklist was completed by the attending physician.
* If there were no exclusion criteria, written informed consent was obtained and baseline information, including initial headache pain score ratings with VAS and...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients were eligible for inclusion if they were aged 18 years or older, 65 years or younger
- • Had acute migraine attack without aura
- • VAS (visual analog scale) score \>50 mm , NRS (Numeric Rating Scale) score \>5
- • Patients whose written consent is obtained by agreeing to participate in the study
- Exclusion Criteria:
- • Those who refuse to participate in the work
- • Patients younger than 18 years or older than 65 years
- • Those who use ergotamine derivative drugs in the last 24 hours
- • Have received analgesics in the last 6 hours
- • Patients with severe liver, kidney, lung and heart failure
- • To have active peptic ulcer bleeding or perforation
- • Have a history of upper gastrointestinal disease
- • To be Pregnancy and breast-feeding
- • Patients of childbearing age who are not using a birth control method.
- • Allergy to medicines used in work
- • Hemodynamically unstable patients
- • Patients with renal transplantation
- • Blood pressure uncontrolled hypertension patients
- • Patients with cerebrovascular disease history
- • Patients with ischemic heart disease or coronary spasm / printzmetal angina
- • Patients with arrhythmia accompanying Wolff-Parkinson-White syndrome or accessory conduits in the heart
- • Patients with Glucose 6 Phosphate Dehydrogenase (G6PD) deficiency
- • Those with other systemic diseases,
- • Patients with a Visual Analogue Scale (VAS) pain score less than 50 mm
- • Illiterates and patients with vision problems
About Pamukkale University
Pamukkale University is a renowned academic institution located in Denizli, Turkey, dedicated to advancing medical research and education. As a clinical trial sponsor, the university leverages its extensive resources and expertise to facilitate innovative studies aimed at improving patient outcomes and contributing to the broader scientific community. With a commitment to ethical standards and regulatory compliance, Pamukkale University fosters collaboration among researchers, healthcare professionals, and industry partners, ensuring the rigorous execution of clinical trials that address critical health challenges. Through its research initiatives, the university aims to enhance the understanding of various medical conditions and support the development of effective therapies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Denizli, , Turkey
Patients applied
Trial Officials
Cuneyt Arikan, MD
Principal Investigator
Pamukkale University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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