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The diagnostic value of MR for spontaneous intracranial hypotension syndrome.

The diagnostic value of MR for spontaneous intracranial hypotension syndrome.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105701
Enrollment
Unknown
Registered
2025-07-09
Start date
2024-05-01
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Spontaneous intracranial hypotension syndrome

Interventions

Spontaneous intracranial hypotension syndrome group:NA
Healthy control group:NA

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient group of spontaneous intracranial hypotension syndrome: 1. Patients clinically diagnosed with spontaneous intracranial hypotension syndrome; 2. MR Plain scan was received before treatment, and the clinical data were complete. Healthy control group: 1. Healthy people matched by age and gender at the physical examination center; 2. Have undergone regular MR Scans and the images are complete.

Exclusion criteria

Exclusion criteria: Patient group with spontaneous intracranial hypotension syndrome:The clinical data and MR Images are incomplete and the image quality is poor. Healthy control group:The clinical data and MR Images were incomplete and the image quality was poor.

Design outcomes

Primary

MeasureTime frame
Subdural effusion;Subdural hematoma;Signs of pituitary pseudotumor;Venous sinus dilatation;Sagging of the brain;Downward displacement of cerebellar tonsils;

Secondary

MeasureTime frame
VOG angle;Distance between the ventral pons;Transverse diameter of the third ventricle;Central sulcus width;Mammillary-pontine distance;Anteroposterior and left-right diameters of venous sinuses;

Countries

China

Contacts

Public ContactXie Guangbin

The First Affiliated Hospital of Nanchang University

xieguangbin@ncu.edu.cn+86 791 88694170

Outcome results

None listed

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