Skip to content

Detection of reflective cerebral capillary damage in patients with central vertigo

Detection of reflective cerebral capillary damage in patients with central vertigo

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107252
Enrollment
Unknown
Registered
2025-08-07
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Patients with central vertigo who have cerebral capillary reactive damage (such as small vessel disease, chronic cerebral ischemia) present with non-rotatory vertigo (floating sensation, imbalance) lasting for several hours, unrelated to body position, and often accompanied by vertical/gaze nystagmus (negative head impulse test). Microcirculatory disorders may cause gait instability (sticky gait),

Interventions

Healthy control group:NA
Central vertigo group:NA

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Central Vertigo Group: Age 18–75 years, no gender restrictions; Meets the diagnostic criteria for central vertigo established by the International Barany Society (2020 edition) and has been diagnosed with central vertigo at our hospital; Vertigo symptoms have persisted for >=1 month, and acute cerebral infarction, hemorrhage, or other structural lesions have been ruled out via cranial MRI or CT; Able to cooperate with MRI scanning and CO2 stimulation testing; Has signed an informed consent form and voluntarily participates in the study. 2. Healthy control group: aged 18–75 years, no gender restrictions; no history of vertigo or neurological disorders; no abnormalities detected on cranial MRI; able to cooperate in completing MRI scans and CO2 stimulation experiments; signed informed consent form and voluntarily participated in the study.

Exclusion criteria

Exclusion criteria: 1. Contraindications for MRI (e.g., metallic implants in the body, claustrophobia); 2. Severe cardiovascular or pulmonary conditions (e.g., chronic obstructive pulmonary disease (COPD), heart failure) or inability to tolerate CO2 stimulation; 3. Pregnant or breastfeeding women; 4. Recent (within 1 month) use of vasoactive medications (e.g., calcium channel blockers, nitrates); 5. inability to cooperate with MRI scanning or respiratory control tasks (e.g., severe cognitive impairment); 6. family history of neurological diseases (e.g., Alzheimer's disease, Parkinson's disease); 7. recent (within 6 months) history of major surgery or trauma.

Design outcomes

Primary

MeasureTime frame
Cerebral vascular reactivity;

Countries

China

Contacts

Public ContactYu Zhao

West China Hospital, Sichuan University

zhaoyu2013022063@163.com+86 19983130859

Outcome results

None listed

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