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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03418766
Other study ID # CAMBRAIN
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 15, 2018
Est. completion date December 30, 2020

Study information

Verified date March 2020
Source First Hospital of Jilin University
Contact Yingqi Xing, MD,PhD
Phone 15844047846
Email xingyq2009@sina.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of the study is to evaluate the prevalence of white matter lesions in Chinese migraineurs with and without right-to-left shunt. The aim is to study the relationship among right-to-left shunt, migraine and white matter lesions.


Description:

This is a prospective multicenter study of Chinese population. Participants (normal individuals without migraine and migraineurs) are included after standardized diagnostic procedures (TCD and migraine diagnosis). For all the participants, brain MRI and c-TCD are required. Up to 10-15 study sites nationwide will be needed to recruit the planned participant population during a 1-year period.

The information of each participants will be registered, including basic facts, the longitudinal headache history, frequency, location, quality, intensity, duration, accompanied symptoms, precipitating and exacerbating factors, with or without aura, and Headache Impact Test-6 (HIT-6) questionnaire.


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date December 30, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- patients who fulfilled the criteria for migraine according to the International Classification of Headache Disorders III-beta were included.

healthy volunteers without a history of migraine were included as controls.

Exclusion Criteria:

- Subjects were excluded from the study if they had severe arterial stenosis, an insufficient temporal window, inadequate cubital venous access, and/or were unable to perform the Valsalva manoeuvre (VM) because of severe heart or lung disease.

Study Design


Locations

Country Name City State
China First hospital of Jilin Uni Changchun Jilin

Sponsors (2)

Lead Sponsor Collaborator
First Hospital of Jilin University National Natural Science Foundation of China

Country where clinical trial is conducted

China, 

References & Publications (1)

Del Sette M, Dinia L, Bonzano L, Roccatagliata L, Finocchi C, Parodi RC, Sivori G, Gandolfo C. White matter lesions in migraine and right-to-left shunt: a conventional and diffusion MRI study. Cephalalgia. 2008 Apr;28(4):376-82. doi: 10.1111/j.1468-2982.2 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary contrast-enhanced transcranial Doppler (c-TCD) Brain MRI 1 year
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