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Search / Trial NCT07070635

Abertay Tea for Cardiovascular Health During Menopause

Launched by ABERTAY UNIVERSITY · Jul 8, 2025

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Seaweed Fermented Menopause Vascular Function Cardiovascular Risk Continuous Non Invasive Arterial Pressure

ClinConnect Summary

This clinical trial is looking at whether drinking a special kind of tea—English breakfast tea mixed with fermented seaweed—can help improve heart and blood vessel health in women who have gone through menopause. Because women’s risk for heart problems often increases after menopause, researchers want to see if the natural compounds in seaweed can lower this risk by improving things like blood pressure and blood vessel function. The tea has been specially made to taste like regular English breakfast tea but contains added seaweed that may offer these heart benefits.

To join the study, you need to be a woman who has not had a menstrual period for at least a year (meaning you are postmenopausal), regularly drinks tea at least once a week, and is willing to drink three cups of this special tea every day for eight weeks. The study is for women with a body weight in a healthy to moderately high range and without a history of serious heart disease, diabetes, cancer, or other specific health issues. Participants will be asked to drink the tea daily and have their heart and blood vessel health checked before and after the eight weeks to see if the tea makes a difference. This study could help find a simple, enjoyable way to support heart health in many women after menopause.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Postmenopausal status: no menstrual period over the last 12 months
  • Regular tea drinkers (at least once a week), willingness to consume 3 cups of English breakfast tea per day for 8 weeks
  • BMI between 18.5 and 39.99 kg/m2
  • Exclusion Criteria:
  • Reported history of CVD (myocardial infarction, angina, venous thrombosis, stroke, dyslipidemia), diabetes (or fasting glucose ≥ 6.1 mmol/L), kidney, liver or bowel disease.
  • Recent history of cancer (\<1y)
  • History indicative of a congenital or acquired platelet or haemostatic defect.
  • Presence of gastrointestinal disorder or use of drug, which is likely to alter gastrointestinal motility or nutrient absorption.
  • Recent use of hypolipidaemic, antiplatelet or antithrombotic medications
  • Impairment of thyroid function
  • Current smokers or vapers
  • Current self-reported weekly alcohol intake exceeding 14 units
  • Current or recent use of hormone replacement therapy (\<3 months)
  • Recent participation in another clinical trial (\<3 months)
  • Allergy or intolerance to crustaceans or iodine

About Abertay University

Abertay University is a reputable higher education institution known for its strong emphasis on applied research and innovation across various disciplines. As a clinical trial sponsor, Abertay University leverages its academic expertise and state-of-the-art facilities to advance scientific knowledge and contribute to the development of evidence-based healthcare solutions. The university is committed to conducting ethically sound and methodologically rigorous clinical studies that aim to improve patient outcomes and support the broader medical community.

Locations

Dundee, , United Kingdom

Patients applied

0 patients applied

Trial Officials

Sarah C Cottin, PhD

Principal Investigator

Abertay University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported