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Clinical observation for the therapeutic effect of mNGF on cognitive decline in cerebral small vessel disease

Clinical observation for the therapeutic effect of mNGF on cognitive decline in cerebral small vessel disease

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021143
Enrollment
Unknown
Registered
2019-01-30
Start date
2018-10-01
Completion date
Unknown
Last updated
2019-02-04

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

Conditions

Cerebral small vessel disease

Interventions

Experimental group:Conventional drugs and cholinesterase inhibitors + mouse nerve growth factor (mNGF)
Control group:Conventional drugs and cholinesterase inhibitors

Sponsors

The First Affiliated Hospital, Sun Sat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 50-80 years old; 2. Clinical symptoms of acute CSVD, including TIA or lacunar infarction, and with related lesions on MRI imaging (acute infarction with diameter = 1), white matter lesion (Fazekas > = 2), cerebral microbleeds (number > =1 in deep white matter), enlarged perivascular space(number > = 10 in basal ganglia); 4. Clinical diagnosis of vascular cognitive impairment or dementia, MMSE score =<26; 5. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Intracranial or extracranial arterial stenosis of > 50% luminal stenosis or prior history of endarterectomy of cerebral large arteries; 2. TOAST classification suggested (very) possible cardioembolic stroke; 3. Large cortical or subcortical infarctsion with diameter > 1.5cm on MRI; White matter lesions caused by other diseases such as multiple sclerosis; Other central nervous system diseases such as cerebral hemorrhage, brain trauma, epilepsy, encephalitis, hydrocephalus or brain tumors; Oher systemic diseases, such as liver and kidney insufficiency, tumor, etc.; 4. History of alcohol intoxication, drug addiction, or mental disease, or severe aphasia; 5. Contraindication for MRI examination.

Design outcomes

Primary

MeasureTime frame
ADAS-cog;

Secondary

MeasureTime frame
MMSE;MoCA scale;digit span test;Activity of Daily Living Scale;Patient Health Questionnaire-9 Score;Hamilton anxiety scale;Hamilton depression scale;

Countries

China

Contacts

Public ContactFan Yuhua

The First Affiliated Hospital, Sun Sat-sen University

fansusan@126.com+86 13600086863

Outcome results

None listed

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