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NCT04912752

Copy Number Variation in CHRNA7 Gene in Migraine and Gene Expression

Completed NA Last updated 3 June 2021
What this trial tests

NA trial testing Migraine CNV in Migraine in 200 participants. Completed in 2 January 2021.

Timeline
5 April 2020
Primary endpoint
10 December 2020
2 January 2021

Quick facts

Lead sponsorUniversity of Gaziantep
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposebasic science
Enrollment200
Start date5 April 2020
Primary completion10 December 2020
Estimated completion2 January 2021
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

University of Gaziantep

Who can join

Eligibility, any sex, with Migraine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Migraine

Currently open trials in the same condition.

Other University of Gaziantep trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04912752.

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