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NCT06989697RecruitingPhase 3

Cilostazol-Ginkgo for Cognitive Function in Elderly Diabetes

Impact of Cilostazol and Ginkgo Leaf Extract on Cognitive Function in Elderly Patients With Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 25 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This exploratory pilot study aims to evaluate the cognitive improvement effects of combination therapy with cilostazol (200 mg) and ginkgo biloba extract (160 mg) in elderly patients with type 2 diabetes mellitus. Both agents have demonstrated potential cognitive benefits through mechanisms such as enhanced cerebral blood flow, anti-inflammatory activity, and neuroprotection. Given the increased risk of cognitive decline and dementia in patients with type 2 diabetes, and the need for preventive strategies, this study will investigate whether the combination therapy can prevent or mitigate cognitive deterioration. Findings from this study may provide foundational data for the future development of therapeutic interventions targeting cognitive impairment in patients with diabetes.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
80 (estimated)
First submitted
29 Apr 2025
Start date
1 Jan 2025
Primary completion date
31 Dec 2026
Lead sponsor
Seoul National University Bundang Hospital
NCT number
NCT06989697

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 80
  • From 1 Jan 2025 to the primary completion date, 31 Dec 2026
  • 1 site in 1 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 requiring antiplatelet or anticoagulant therapy other than the investigational product
  • Patients with a history of alcohol or drug abuse within 1 year prior to screening
  • Patients with a history of taking medications that may affect cognitive function within 3 months prior to screening

Other illness

  • Patients with type 1 diabetes mellitus, diabetic ketoacidosis, or diabetic coma or precoma
  • Patients diagnosed with dementia (e.g., Alzheimer's disease)
  • Patients with suspected cognitive impairment due to other causes
  • Patients with severe infections, recent surgery (perioperative status), or major trauma
  • Patients with pituitary or adrenal insufficiency
  • Patients with other medical conditions requiring hospitalization

Lab values

  • Patients with poorly controlled blood glucose (HbA1c \> 10.0%)

Other

  • Patients with an MMSE score below 24
  • Patients with thyroid dysfunction requiring treatment (i.e., abnormal TSH levels)
  • Patients with severe depression
  • Patients deemed by the investigator to be otherwise unsuitable for study participation

Who the study is looking for

  • Patients diagnosed with type 2 diabetes mellitus
  • Adults aged 60 years or older
  • Patients with a Mini-Mental State Examination (MMSE) score between 24 and 28 within the past 3 months

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Seoul National University Bundang Hospital
Coordinator of this site? Confirm its status
Seongnam-siSouth KoreaRecruiting

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