Actively Recruiting

Phase Not Applicable
Age: 50Years - 85Years
All Genders
NCT07334366

Broccoli Sprout Extract for Cognitive Function

Led by Pusan National University Yangsan Hospital · Updated on 2026-01-13

100

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This clinical trial aims to determine whether broccoli sprout extract improves cognitive function in adults with mild cognitive impairment and to assess its safety. The main questions are: * Does broccoli sprout extract improve cognitive function in participants? * What side effects occur when participants take broccoli sprout extract?

CONDITIONS

Official Title

Broccoli Sprout Extract for Cognitive Function

Who Can Participate

Age: 50Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 55 to 85 years, both male and female
  • Global Deterioration Scale (GDS) score of 2 or 3 (subjective or mild objective memory impairment)
  • No diagnosis of dementia according to established criteria
  • Ability to read Korean
Not Eligible

You will not qualify if you...

  • Severe medical conditions within the past 6 months such as severe cerebrovascular disease, cardiac disease requiring treatment, or malignancy (stable cases may be allowed at investigator's discretion)
  • Diseases associated with cognitive impairment including dementia, Parkinson's disease, cerebral infarction, or other cognitive decline conditions
  • Uncontrolled hypertension with blood pressure 160/100 mmHg or higher after resting 10 minutes
  • Poor glycemic control with fasting blood glucose 160 mg/dL or higher in diabetic patients
  • Uncontrolled thyroid dysfunction under treatment
  • Renal impairment with serum creatinine twice the upper limit of normal
  • Hepatic impairment with AST or ALT twice the upper limit of normal
  • Severe gastrointestinal symptoms such as severe heartburn or dyspepsia
  • Use of medications or health foods affecting cognitive function within the past month
  • Participation in other drug clinical trials within the past month or planned during the study
  • Severe alcohol use disorder
  • Known allergies to study product components
  • Any other conditions deemed inappropriate by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Pusan National University Yangsan Hospital

Yangsan, South Korea, 50612

Actively Recruiting

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Research Team

S

Sang Yeoup Lee, Professor, MD, PhD

CONTACT

Y

Ye Li Lee

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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