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Precise diagnosis and treatment of neural system diseases related to patent foramen ovale based on multi-omics study

Precise diagnosis and treatment of neural system diseases related to patent foramen ovale based on multi-omics study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069620
Enrollment
Unknown
Registered
2023-03-22
Start date
2023-03-22
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Episodic diseases of the nervous system

Interventions

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18-50 years old, male or female; (2) Comply with the 2018 International Society's Headache Classification Third Edition (ICHD-III) diagnostic criteria for migraine, comply with the International Anti Epilepsy Alliance (ILAE) diagnostic criteria for epilepsy (2014), and control subjects (without migraine or epilepsy); (3) Voluntarily sign a written informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with severe cardiovascular diseases (severe heart failure, atrial fibrillation, after cardiovascular intervention surgery) and cerebrovascular diseases (stroke, cerebrovascular malformations), central nervous system infections, intracranial space occupying lesions, or brain trauma; (2) Secondary epilepsy; (3) People with metabolic diseases such as diabetes; (4) Patients with severe primary diseases of the liver and renal hematopoietic system or severe liver or renal insufficiency (transaminase exceeding 3 times the upper limit of normal value, total bilirubin and creatinine exceeding 1.5 times the upper limit of normal value, or creatinine clearance rate<45ml/min); (5) Migraine patients or controls who took any medication 1 week before the examination; (6) Planned pregnancy, pregnancy, and lactation women; (7) Participants in other clinical intervention trials; (8) Other situations judged by the researcher to be unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Metabolomics;Proteomics;

Secondary

MeasureTime frame
Exosomes;MRI;

Countries

China

Contacts

Public ContactLei Chen

West China Hospital, Sichuan University

leilei_25@126.com18980605819

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026