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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01358279
Other study ID # 2009-4615-A
Secondary ID
Status Completed
Phase N/A
First received May 18, 2011
Last updated October 23, 2016
Start date January 2009
Est. completion date March 2011

Study information

Verified date October 2016
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority South Korea: Korea Food and Drug Administration (KFDA)
Study type Interventional

Clinical Trial Summary

This study is conducted to investigate the therapeutic efficacy and safety of transcranial direct current stimulation (tDCS) over the primary motor cortex of patients with acute migraine attack.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date March 2011
Est. primary completion date October 2009
Accepts healthy volunteers No
Gender Both
Age group 17 Years to 70 Years
Eligibility Inclusion Criteria:

- Aged 17-70 years

- Migraine

- With or without aura

- The first attack of migraine was earlier than 50 years of age

- One to 8 moderate to severe migraine attacks per month in the 2 months preceding the screening

- Willing and able to give written informed consent

- Able to read, comprehend and complete the diary form

Exclusion Criteria:

- Not able to distinguish between migraine and non-migraine headache

- Combined headache, including the tension type headache and medication overuse headache

- Pregnant, actively trying to become pregnant or breast-feeding women

- Uncontrolled and significant medical illness

- Vertebrobasilar or hemiplegic migraine according to the International Headache Society diagnostic criteria

- Having intracranial metal implants or a cardiac pacemaker

- A history of epilepsy or other organic brain disorders

- A history of psychological diseases

- Having changed medications for migraine within 1 month before giving us informed consent

- Drug abuser or alcoholics

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
transcranial direct current stimulation
A constant current of 2 mA intensity applied for 20 min over C3 or C4

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants who experienced pain relief of one level or more at 2h post-treatment No
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