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Antihistamines in migraine Prophylaxis

“COMPARISON OF EFFICACY AND TOLERABILITY OF LEVOCETIRIZINE WITH MONTELUKAST-LEVOCETIRIZINE COMBINATION AS AN ADD-ON THERAPY IN MIGRAINE PROPHYLAXIS?,-An open label, Prospective, Comparative Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/038228
Enrollment
90
Registered
2021-11-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G431- Migraine with aura

Interventions

Intervention1: Propranolol, Amitryptyline, Sodium Valproate, Levocetirizine: T.Propranolol 40mg/T. Amitriptyline 25mg/T. Sodium Valproate 200mg They can be given either as single or in combination the

Sponsors

Madras medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with Migraine headache as per ICHD-3 criteria Patients fulfilling the criteria for the prophylaxis of Migraine Age group of 18-60 years of age Sex- Both male and female Patients who are willing to participate in this study

Exclusion criteria

Exclusion criteria: Patients with headache other than migraine Patients with complicated migraine like ophthalmic, hemiplegic or migraine with brainstem aura Patients with H/O severe drug allergy Patients with H/O severe co-morbidities like hypertension, Coronary artery disease, uncontrolled Diabetes Mellitus, thyroid disease, renal or liver disease, asthma. H/O any drug abuse or drug dependence Patients with H/O any psychiatric illness Pregnant ladies, lactating mothers and children less than 18 years of age

Design outcomes

Primary

MeasureTime frame
End points of the study1.Proportion of patients with 50% reduction in frequency of attacks at the end of 3rd month of the study Timepoint: At 3rd month of study

Secondary

MeasureTime frame
To assess the reduction in frequency and severity of pain intensity at the end of 6th month of the study To observe for any adverse effect with study drugTimepoint: At 6 months of study

Countries

India

Contacts

Public ContactDr Chenthamarai

Institute of Pharmacology, Madras Medical College

gchenthamarai@gmail.com9445656912

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026