Comparison of Oral Paracetamol and Zolmitriptan Efficacy in the Treatment of Acute Migraine in Emergency Department

Pamukkale University

Status and phase

Completed

Phase 4

Conditions

Acute Migraine Headache

Treatments

Drug: Zolmitriptan

Drug: Paracetamol

Study type

Interventional

Funder types

Other

Identifiers

NCT03145467

2015TPF039

Details and patient eligibility

About

Migraine is a chronic and sometimes progressive disorder, characterized by headache, recurrent episodes, and other associated symptoms. Migraine is the most common cause of headache among patients who applied to emergency services.

The purpose of the investigators is to compare the efficacy of oral paracetamol and zolmitriptan in the treatment of acute migraine headache in an emergency department.

Full description

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 NRS were recorded.
The need for identification and enrollment of participants by staff with conflicting work pressures resulted in recruitment of a convenience sample of patients.
All patients eligible for the study were randomized to one of two groups:
First Group: paracetamol 1000 mg was given oral to 100 patients,
Second Group: Zolmitriptan 2,5 mg was given oral to 100 patients which determined to be applied as a group.
Drugs were prepared according to the computer-generated random number sequence to assign treatment allocations.
The allocation list was kept by the emergency nurse. Patients received the paracetamol, zolmitriptan medication schemes according to their random allocations.
After enrollment and recording of baseline information, the next numbered study drug was obtained, and administered as oral.
Randomization was achieved by using computer software to generate random numbers. During the intervention, participants were monitored by an oxygen saturation (SpO2) monitor, an automatic sphygmomanometer (blood pressure), and a rhythm monitor (heart rate and rhythms)
One researcher blinded to patient allocation observed the whole procedure and recorded the Headache scores.
Headache scores were recorded at 0, 15, 30, and 60 min on a VAS of 1 to 100 mm and NRS of 1 to 10. Patients with nausea are treated with 15 minutes of 10 mg metoclorpramide slow infusion in 150 cc saline solution.
Rescue medication (1 mcg/kg fentanyl ) was given İntravenöz to patients if pain VAS scores ≥ 50 mm in 60 minutes after study drug administration.
All other medications required during the study also were recorded.
During the study, pulse rate, systolic blood pressure, diastolic blood pressure, respiration rate and oxygen saturation (SpO2) were recorded at baseline (0 min), 15, 30, and 60 min.

Enrollment

200 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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