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SCREEN-HFI (SCReening Evaluation of the Evolution of New Heart Failure Intervention Study)

M

Monash University

Status and phase

Completed
Phase 3

Conditions

Heart Failure

Treatments

Drug: Placebo
Drug: Spironolactone

Study type

Interventional

Funder types

Other

Identifiers

NCT00604006
CP-02/07

Details and patient eligibility

About

Individuals who were a part of the investigators Screen-HF study (NCT00400257) whose BNP level are in the top quintile will be offered participation in this study. Participants will be randomised to receive either spironolactone or placebo for three years. Participants will then be monitored for indications of heart failure. It is anticipated that the medication will reduce the development of heart failure in this group.

Enrollment

20 patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Was recruited to SCREEN-HF
  2. Has provided informed consent

Exclusion criteria

  1. Uncorrected hyperkalaemia
  2. eGFR < 30 ml/min

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

20 participants in 2 patient groups, including a placebo group

Group A
Experimental group
Treatment:
Drug: Spironolactone
Group B
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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