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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04912752
Other study ID # 2020/12
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 5, 2020
Est. completion date January 2, 2021

Study information

Verified date May 2021
Source University of Gaziantep
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Migraine is a common and possible hereditary disease. Copy number variation (CNV) is a phenomenon in which parts of the genome are repeated and the number of repeats in the genome varies between individuals in the human population.The CHRNA7 gene has a major role in the neuropsychiatric phenotypes observed in patients. The 15q13.3 gain/loss variation in this gene may be associated with migraine.


Description:

Migraine is a common neurological disorder. Although they have different genetic bases according to their types, cholinergic receptors after calcium channels play an important role in the clinic and genetics of the disease. Neuronal acetylcholine receptor subunit alpha-7, also known as nAChRα7, is a protein that in humans is encoded by the CHRNA7 gene.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date January 2, 2021
Est. primary completion date December 10, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Migraine Exclusion Criteria: Vascular problems

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Migraine CNV
Copy number variation effect on migraine disease

Locations

Country Name City State
Turkey Medicine Gaziantep Sehitkamil

Sponsors (1)

Lead Sponsor Collaborator
University of Gaziantep

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary CNV number CNV number effect on migraine 1 year
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