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Effect of Pentoxifylline on Cognitive Impairment After Ischemic Stroke

H

Hebei Medical University

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Cognitive Impairment

Treatments

Drug: Pentoxifylline

Study type

Interventional

Funder types

Other

Identifiers

NCT06344390
20210327

Details and patient eligibility

About

Pentoxifylline can improve cognitive impairment after ischemic stroke, possibly by improving the level of cerebral blood flow, affecting the content of blood oxygen and metabolic substances in the brain, and then playing a protective role in the transmission of nerve electrical signals, and ultimately improving cognitive function. The patients with cognitive impairment and non-dementia PSCIND after ischemic stroke were randomly divided into two groups. In addition to the basic drugs of ischemic stroke, the patients were given pentothemine sustained release tablets and blank control respectively to observe the effects of pentothemine on cognitive function and neuronal electrical signals in the patients with ischemic PSCIND. It is expected to explore the possible internal biological mechanism by using transcranial Doppler, oxygen-dependent functional magnetic resonance imaging and craniocerebral magnetic resonance pop analysis. Finally, statistical correlation analysis was used to elucidate the specific mechanism of pentoxifylline in improving cognitive function of non-dementia patients with cognitive impairment after ischemic stroke.

Full description

Pentoxifylline can improve cognitive impairment after ischemic stroke, possibly by improving the level of cerebral blood flow, affecting the content of blood oxygen and metabolic substances in the brain, and then playing a protective role in the transmission of nerve electrical signals, and ultimately improving cognitive function.

Enrollment

200 estimated patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Han Chinese, age 40-80 years old, male and female, right-handed;
  • The diagnosis is consistent with the Expert Consensus on the Management of Cognitive Impairment after Stroke 2021;
  • NIHSS score 1-15 points;
  • Daily Living Ability Scale (ADL) ≥75 score;
  • The Informed consent signed by the patient or his legal representative

Exclusion criteria

  • Can not cooperate with the examination (including neuropsychological tests and scale assessment);
  • There were memory disorders, dementia with lewy bodies and frontotemporal dementia before the onset of stroke events;
  • There were definite infectious diseases 2 weeks before admission; Have a serious mental illness, previous history of cancer, alcohol or drug abuse;
  • Use of drugs that may affect cognitive function, including sedatives, anti-anxiety drugs, hypnotics, nootropic drugs, and cholinoid drugs;
  • Can not accept brain MRI examination

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

200 participants in 2 patient groups

Pentoxifylline
Experimental group
Description:
Pentoxifylline
Treatment:
Drug: Pentoxifylline
No intervention
No Intervention group
Description:
No intervention

Trial contacts and locations

1

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Central trial contact

Bing Han, Ph.D. degree; Jiaying Rong, master

Data sourced from clinicaltrials.gov

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