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NCT06795438

Effects of Green Tea on Cardiometabolic Outcomes

Not yet recruiting NA Last updated 27 March 2025
What this trial tests

NA trial testing Green tea in Cardiometabolic Syndrome in 40 participants. Not yet recruiting.

Timeline
1 April 2025
Primary endpoint
1 February 2027
1 June 2027

Quick facts

Lead sponsorUniversity of Central Lancashire
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment40
Start date1 April 2025
Primary completion1 February 2027
Estimated completion1 June 2027
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

University of Central Lancashire

Who can join

Adults 18 to 65, any sex, with Cardiometabolic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Cardiovascular disease, type 2 diabetes mellitus and associated diseases combined are the leading health burden and cause of mortality worldwide; therefore, the necessity for an intervention is paramount. Dietary interventions to improve cardiometabolic health are highly sought after as they possess less risk than pharmacological drugs. It has been postulated that Green tea may be beneficial in improving cardiometabolic outcomes. However, to date, no research has explored this using a placebo randomized intervention.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Green tea

Trials testing the same drug.

Other recruiting trials for Cardiometabolic Syndrome

Currently open trials in the same condition.

Other University of Central Lancashire trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06795438.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing