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RECRUITING
NCT04286399
PHASE4

Asian Diabetes Outcomes Prevention Trial

Sponsor: National Heart Centre Singapore

View on ClinicalTrials.gov

Summary

The aim of this study is to identify patients with DM at high risk of CVD using elevated N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels (\>125pg/mL), and (2) intensify therapy using renin-angiotensin system (RAS) antagonists, beta-blockers and sodium glucose co-transporter-2 inhibitors (SGLT2i) for primary prevention of cardiovascular events in this high-risk DM population.

Key Details

Gender

All

Age Range

40 Years - Any

Study Type

INTERVENTIONAL

Enrollment

2400

Start Date

2019-07-01

Completion Date

2034-06-30

Last Updated

2021-04-30

Healthy Volunteers

No

Interventions

DRUG

Renin-angiotensin-aldosterone system inhibitors

Research participants in the intensive therapy arm should be strongly encouraged to follow the intensive treatment strategy. Every attempt should be made to up-titrate RAS-antagonists and beta-blockers (max dosage, unless contraindicated) as well as preferentially use SGLT2i (standard dosage, as required) throughout the trial.

DRUG

Beta blocker

Research participants in the intensive therapy arm should be strongly encouraged to follow the intensive treatment strategy. Every attempt should be made to up-titrate RAS-antagonists and beta-blockers (max dosage, unless contraindicated) as well as preferentially use SGLT2i (standard dosage, as required) throughout the trial.

DRUG

SGLT2 Inhibitor - Sodium Glucose Cotransporter Subtype 2 Inhibitor Product

Research participants in the intensive therapy arm should be strongly encouraged to follow the intensive treatment strategy. Every attempt should be made to up-titrate RAS-antagonists and beta-blockers (max dosage, unless contraindicated) as well as preferentially use SGLT2i (standard dosage, as required) throughout the trial.

Locations (1)

Singapore General Hospital (SGH)

Singapore, Singapore