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NCT06237062 | NOT YET RECRUITING | Migraine

Migraine Survey in Gulf Region

Novartis Pharmaceuticals

Brief Summary:

The objective of this study is to evaluate the effect of erenumab on medication-specific treatment satisfaction in patients newly started on erenumab over 12 weeks

Condition or disease




Detailed Description:

This is a longitudinal prospective descriptive primary data collection using a 20 min online survey. Patients will be selected by investigators (general neurologists, headache/migraine specialists) in primary care clinics and hospitals. After fulfilling the inclusion criteria, the patient will be asked to sign an online informed consent. A 5 min screener will follow after which the patient will be directed through a link to the full survey. The duration of data collection will be for 6 months since the start of survey rolling in each site across centers in the Gulf Region.

Estimated Enrollment : 200 participants
Official Title : Real-world Experience of Patients Newly Started on Erenumab in the Gulf Region: a Longitudinal Prospective Observational Study
Actual Study Start Date : 2024-06-30
Estimated Primary Completion Date : 2025-03-30
Estimated Study Completion Date : 2025-03-30

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years to 100 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Inclusion Criteria
  • * EM\& CM (with or without Medication Overuse Headache (MOH)) patients
  • * Newly Started on erenumab either 70 mg or 140 mg (first dose received within 1 month prior study enrollment and baseline endpoints collection)
  • * Ability to receive 3 monthly doses of erenumab.
  • * Age more than 18 years
  • * Males and Females
  • * Allowing the patients to be stable on 1 adjunctive migraine preventive medication (if present)
  • * Agreed to be included in the study and signed informed consent
Exclusion Criteria
  • * Less than 18 years
  • * Age at onset of Migraine more than 50 years
  • * Any contraindications to the start of erenumab as per label
  • * Refusal to sign informed consent
  • * Inability to participate or restricted access to the online survey
  • * Enrolled in an interventional migraine-related study at the time of the study enrollement

Migraine Survey in Gulf Region

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