RecruitingPhase 2NCT06889753

A Clinical Trial to Investigate the Effect of Pollen Extracts on Menopausal Symptoms in Healthy Women.

A Randomized, Triple-blind, Placebo Controlled, Parallel Clinical Trial to Investigate the Effect of Pollen Extracts on Menopausal Symptoms in Healthy Women.


Sponsor

Graminex LLC

Enrollment

120 participants

Start Date

Oct 29, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this study is to investigate the effect of pollen extracts on menopausal symptoms in healthy women The main question it aims to answer is: What is the difference in change in severity of menopausal symptoms as assessed by the total Menopause Rating Scale (MRS) score from baseline at Week 36 between Graminex Water Soluble Pollen Extract (WSPE), Lipid Soluble Pollen Extract (LSPE), and Placebo? Participants will be asked to complete the MRS assessment tool to rate their menopausal symptoms while receiving either WSPE, LSPE, or Placebo.


Eligibility

Sex: FEMALEMin Age: 45 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Graminex LSPE, Graminex WSPE, and others for people with menopausal women. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTGraminex WSPE

Graminex Water Soluble Pollen Extract is standardized to 6% amino acids.

DIETARY_SUPPLEMENTGraminex LSPE

Graminex Lipid Soluble Pollen Extract is standardized to 7% phytosterols.

DIETARY_SUPPLEMENTPlacebo

Placebo


Locations(1)

KGK Science Inc.

London, Ontario, Canada

View Full Details on ClinicalTrials.gov

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NCT06889753


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