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NCT06140888Not yet recruiting

Effect of Ginkgo Biloba Extract on Cognitive Function in Acute Ischemic Stroke

Effect of Ginkgo Biloba Extract on Cognitive Function in Acute Ischemic Stroke: a Multicentre, Randomised, Open-label, Blinded-Endpoint Trial

Source: ClinicalTrials.gov · Last updated 28 Feb 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to determine the effect of ginkgo biloba extract on cognitive function in acute ischemic stroke.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
356 (estimated)
First submitted
15 Nov 2023
Start date
15 Mar 2024
Primary completion date
1 Oct 2026
Lead sponsor
Yi Yang
Diseases
Stroke
NCT number
NCT06140888

What you commit to

  • Study type: Interventional
  • Planned participants: 356
  • From 15 Mar 2024 to the primary completion date, 1 Oct 2026
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who received emergency reperfusion therapy (including intravenous thrombolysis and endovascular thrombectomy) at onset;
  • Currently using psychoactive medications (e.g., antidepressants) or anti-epileptic drugs, or if the time since their last use of these medications was less than 5 half-lives (per the pharmacokinetics of each specific medication; for drugs with unknown half-lives, a 1 month washout period was required);
  • Currently taking medications intended to improve cognitive function or prevent dementia (e.g., cholinesterase inhibitors, memantine, nootropics), or if the washout period since their last use of these medications was less than 5 half-lives as specified in each drug's pharmacokinetics. For drugs with unknown half-lives, a minimum 1 month washout period was required;
  • Those who are participating in other clinical investigators, or who have participated in other clinical studies within 3 months prior to enrollment;

Other illness

  • Combined with other neurological diseases, such as neurodegenerative diseases (e.g., Alzheimer's disease, Parkinson's disease, Lewy body dementia, and frontotemporal dementia), optic neuritis, epilepsy, central nervous system infections (e.g., AIDS and syphilis), traumatic brain injury dementia, etc;
  • Had a pre-existing diagnosis of a cognitive disorder;
  • Active ulcer or bleeding diathesis;
  • Allergy to preparations containing ginkgo biloba extract;
  • Other conditions that the investigators deemed unsuitable for enrollment.

Other

  • Transient ischemic attack;
  • Severe liver and kidney dysfunction;
  • Pregnant or lactating women, patients with a life expectancy less than 6 months, and those unable to complete the study for other reason;
  • Unwillingness to be followed up or poor treatment compliance;

Who the study is looking for

  • Patients with a definitive clinical diagnosis of acute ischemic stroke;
  • Age≥18 years, regardless of sex;
  • Primary education level or higher; baseline MoCA score of 10-25 points;
  • Able to complete cognitive scale scoring;
  • Informed consent is signed and ginkgo biloba extract therapy is initiated within 14 days of onset.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.