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Clinical study of pentoxifylline on the improvement of cognitive function related to white matter injury in small cerebral vascular disease

Clinical study of pentoxifylline on the improvement of cognitive function related to white matter injury in small cerebral vascular disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069867
Enrollment
Unknown
Registered
2023-03-28
Start date
2023-04-01
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

Cerebral Small Vessel Disease

Interventions

Test group :pentoxifylline sustained-release tablets
Control group:Recommended drugs in the Chinese Guidelines for Diagnosis and Treatment of Cognitive Disorders Related to Cerebrovascular Diseases, 2019

Sponsors

Nanjing Drum Tower hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ( 1 ) Over 60 years old, regardless of gender ; ( 2 ) Clinically diagnosed as cerebral small vessel disease, there are white matter high signal ( Fazekas score 2 points and above ), and cognitive impairment ( MOCA illiteracy = 13 points, 1-6 years of education = 19 points, 7 years or more = 25 points ) ; ( 3 ) The patient himself or his legal representative signed informed consent.

Exclusion criteria

Exclusion criteria: ( 1 ) bleeding tendency : extensive retinal hemorrhage, intracranial hemorrhagic diseases ( such as hemorrhagic stroke, epidural hematoma, subarachnoid hemorrhage, etc. ), brain tumors, tumor stroke, long-term use of anticoagulant drugs ; ( 2 ) Has a clear history of cognitive impairment caused by other reasons, such as ischemic stroke, normal intracranial pressure hydrocephalus, Alzheimer 's disease, Parkinson 's disease, multiple sclerosis, encephalitis, etc. ; ( 3 ) patients with acute myocardial infarction and severe coronary atherosclerosis ; ( 4 ) severe liver dysfunction, renal insufficiency or severe cardiac insufficiency ; ( 5 ) Persons known to be allergic to pentoxifylline and methylxanthines ( such as caffeine, aminophylline, dihydroxypropyl theophylline, etc. ) ; ( 6 ) Other life-threatening or serious diseases, expected survival time < 36 months ; ( 7 ) Researchers believe that the subjects have potential risks or any other factors that interfere with the subjects, and are not suitable for participants in this trial.

Design outcomes

Primary

MeasureTime frame
FLAIR;

Secondary

MeasureTime frame
Mini-Mental State Examination,MMSE;Montreal Cognitive Assessment, MoCA;digital span test, DST;trail making test, TMT-B;Activity of Daily Living, ADL;

Countries

China

Contacts

Public ContactXu yun

Nanjing Drum Tower hospital

xuyun20042001@aliyun.com13914764479

Outcome results

None listed

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