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The effect of magnetic stimulation over scalp in patients suffering from migraine.

The effect of intermittent theta burst repetitive transcranial magnetic stimulation in the treatment of chronic migraine: A double-blind sham-controlled trial. -

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063354
Enrollment
60
Registered
2024-02-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: G43- Migraine

Interventions

Intervention1: Intermittent theta burst repetitive transcranial magnetic stimulation: Active group: active coils using stimulus intensity of 80% of MT, with Frequency-50 Hz, burst frequency-5Hz, deliv

Sponsors

Sujita Singh
Lead Sponsor
Ajay Kumar
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with migraine, diagnosed according to the International Classification of Headache Disorders (ICHD-3rd edition) 2.Age between 18-60 years 3.Sex: all gender 4.Written informed consent for the study obtained from the participants. 5.With or without any prophylactic treatment.

Exclusion criteria

Exclusion criteria: 1.Any other type of chronic or recurrent headache such as diagnosed as sinusitis, refractive errors, cervical spondylosis, and neurological conditions. 2.Neuropsychiatry disorders Organic brain conditions, History of severe head injury, epilepsy, space occupying lesion, trigeminal neuralgia, hydrocephalous, meningitis, and other pain conditions. 3.Otherwise physically healthy conditions 4.Psychogenic pain, tension headache, Somatoform pain disorder 5.Use of botulinum toxin in head or neck region in last 6 months. 6.Active phase of any major Psychiatry illness (Schizophrenia, Bipolar disorder), substance use disorder (except moderate tea and nicotine use). 7.Active phase of depression 8.Confirmed Pregnancy • Having cochlear implant, cardiac pacemaker and metal body implanted in the body.

Design outcomes

Primary

MeasureTime frame
reduction in migraine days, frequency, severity, and duration in migraine in chronic migraine patientTimepoint: patient is assessed for severity, intensity, and duration of migraine by MIDAS, Headache Impact Test-6 (HIT-6)and migraine dairy at 4th, 6th, and 12th week of post-intervention period

Secondary

MeasureTime frame
To compare the improvement from the bassline in intensity of migraine attacks and burden of drugs used for the episode of migraine in the active rTMS and sham rTMS group.Timepoint: 4th,6th and 12th week of post intervention period

Countries

India

Contacts

Public ContactDr Sujita Singh

AIIMS, Raipur

ajaypgimer2016@gmail.com8210686303

Outcome results

None listed

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