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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03484871
Other study ID # 2016-04-028
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date May 2016
Est. completion date April 2019

Study information

Verified date March 2020
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether reduced frequency of migraine attacks are associated with signal alternation and connectivity of cerebral cortex.


Description:

Patients with migraine show reduced cortical thickness in regions subserving pain processing, and it is related to increasing headache frequency. In the past, only one study has shown a reversibility consequence of chronic nociceptive transmission, which normalizes when the pain is adequately treated. However, little is known whether these changes predispose to migraine or represent the effect of repeated migraine attacks. Our region of interest is reduced frequency of migraine attacks are associated with reversibility of signal alternation and functional connectivity of cerebral cortex.

In 30 migraineurs with 8-14days with headache per months who already performed brain magnetic resonance imaging will be recruited. Treatment medications such as frovatriptan and topiramate will be used for 6 months. After 6 months, follow-up brain magnetic resonance imaging will be performed.

The primary outcome is the longitudinal changes in functional connectivity in pain-processing/modulating brain regions. The secondary outcome is following: 1)longitudinal changes in structural and morphological alterations in brain regions of pain processing; 2)structural, morphological, and functional correlates of treatment response; 3)changes in monthly migraine days, migraine frequecies, headache days, and headache frequencies after treatment; 4)responses to acute migraine treatment.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date April 2019
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Premenopausal Women

- Aged 18-50

- Drug-naïve high frequency episodic migraineurs (8-14 attacks/m)

- Performed a baseline interictal brain MRI

Exclusion Criteria:

- Medication overuse

- Chronic pain other than migraine

- On treatment of major depression, bipolar, schizophrenia, or BDI>25

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Samsung Medical Center Seoul

Sponsors (2)

Lead Sponsor Collaborator
Samsung Medical Center SK Chemicals Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary functional MRI imaging changes temporal changes in BOLD correlations in the regions of most significant correlation with periaqueductal grey; temporal changes in BOLD correlations in the regions of most significant correlation with anterior cingulate cortex; temporal changes in default mode network 6 month
Secondary structural MRI imaging changes changes in cortical thickness of anterior cingulate, amygdala, periquiductal grey, and sensorimotor cortex 6 months
Secondary Functional and structural correlates of treatment response >50% reduction of monthly headache days 6 months
Secondary correlation of functional MRI changes with changes in clinical parameters changes in monthly headache days 6 months
Secondary responses to acute migraine treatment the Migraine Assessment of Current Therapy (Migraine-ACT) = 4 6 months after the first visit
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