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Development and Evaluation of a Cognitive Enhancement Product Made From Selected Thai Herbs for Menopausal Women

NCT02567760 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-03-01

No results posted yet for this study

Summary

This study is set up to determine the cognitive enhancing effect and consumption safety of the novel cognitive enhancement product made from the combined extract of Z. mays (purple color) and P. amaryllifolius based-drink (MP1) in menopausal volunteer.

Conditions

  • Healthy

Interventions

DIETARY_SUPPLEMENT

MP1

Subjects receive MP1 drink at the dose of 400 mg/day after meal for 8 weeks.

OTHER

Placebo

Subjects receive Placebo drink after meal for 8 weeks.

Sponsors & Collaborators

  • Khon Kaen University

    lead OTHER

Principal Investigators

  • Jintanaporn Wattanathorn, PhD · Khon Kaen University

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
45 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2016-01-31
Completion
2016-01-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02567760 on ClinicalTrials.gov