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Comparing Subcutaneous Sumatriptan, intravenous Acetaminophen and intravenous Ketorolac efficacy in pain releasing for patients with acute migraine headache and the influence on patients' satisfactio

Phase 2
Recruiting
Conditions
Acute Migraine Headache.
Migraine
Registration Number
IRCT20110814007327N8
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients aged 18-65 with a history of at least one year of migraine headache (with or without aura) with a history of 1 to 6 headache attacks of moderate to severe intensity per month in the 2 months prior to screening.

Exclusion Criteria

Patients with a history of congenital heart diseases.
People with cardiovascular (such as angina and other atherosclerotic diseases) and/or lung diseases.
Patients with cardiac arrhythmias even while under treatment.
Patients suffering from cerebrovascular diseases (stroke, TIA and epilepsy).
Patients suffering from ischemic bowel disease.
people having renal or hepatic failure.
Patients who have a history of alcohol or other substance abuse one year prior to the study.
Presence of any symptoms suggesting neurological defects and/or other neurological pathologies.
women who, are pregnant and/or breastfeed.
patients who use OCPs.
Patients who have asthma.
People with a known allergy to Sumatriptan and/or non-steroidal anti-inflammatory drugs.
Patients suffering from coagulopathies.
Patients having a history of basilar migraines and/or of hemiplegic migraines.
patients suffering from cluster headaches.
Patients who have a previous association with health care system, or are currently working as a health care provider (due to disturbing the blinding process.)
patients with an uncontrolled blood pressure (160 or more systole, distal 95 or more).
patients who smoke.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Satisfaction with headache control. Timepoint: hourly. Method of measurement: questionnaire.;Satisfaction with the control of accompanying symptoms. Timepoint: hourly. Method of measurement: questionnaire.
Secondary Outcome Measures
NameTimeMethod
Headache control. Timepoint: hourly. Method of measurement: Visual Analog pain scale.
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