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Clinical Trials/KCT0007338
KCT0007338
Recruiting
未知

A 12 weeks, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Gastrodia elata Blume and Glycyrrhiza uralensis Fischer extracts mixture on improvement of Cognitive(memory) Function

Wonkwang University, Gwangju Medical Center0 sites100 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Wonkwang University, Gwangju Medical Center
Enrollment
100
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Wonkwang University, Gwangju Medical Center

Eligibility Criteria

Inclusion Criteria

  • 1\) Those who complain of subjective memory loss {one or more points in the subjective memory loss questionnaire (SMCQ)}
  • 2\) Those who Korean\-Mini Mental State Examination(K\-MMSE) results in 18\~28 scores
  • 3\) Participants who have fully understand the information provided about the study voluntarily decided to participate and agree to comply with precautions.

Exclusion Criteria

  • 1\)Patients with a clinically significant disease requiring treatment (i.e., acute or chronic cardiovascular system, endocrine system, immune system, respiratory system, kidney and urinary system, neuropsychiatric system, musculoskeletal inflammation, inflammatory disease, blood and tumor disease, gastrointestinal disease, etc.)
  • 2\)Patients with a history of antipsychotic medication use within 3 months prior to the screening examination
  • 3\)Patients with a history of clinically significant hypersensitivity reactions to drugs and test products
  • 4\)Patients who have participated in other clinical trials within 3 months prior to the screening examination
  • 5\)Patients with a Severe score of 29\-63 points as a result of the Depression Scale (BDI) test
  • 6\)Patients who are judged ineligible to participate in the trial by the principal investigator for other reasons, including laboratory test outcomes

Outcomes

Primary Outcomes

Not specified

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