Skip to main content
Clinical Trials/NCT04554277
NCT04554277
Recruiting
Not Applicable

Medico-economic Evaluation of Therapeutic Adaptation Guided by the Soluble Suppression of Tumorigenicity 2 (sST-2) Biomarker in the Management of Patients With Acute Heart Failure

University Hospital, Montpellier12 sites in 1 country710 target enrollmentApril 27, 2021

Overview

Phase
Not Applicable
Intervention
Biomarker guided therapy
Conditions
Heart Failure
Sponsor
University Hospital, Montpellier
Enrollment
710
Locations
12
Primary Endpoint
Cost-utility ratio
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

Management of patients with heart Failure remains a major health concern because of the high rate of rehospitalization, mortality and induced-cost. Biomarkers could help to guide the management of patients with heart failure (HF). Soluble suppression of tumorigenicity 2 (sST2) appears as a promising biomarker. As a working hypothesis, we postulate that sST2 values monitoring could be an helpful guide for medical management in an attempt to reduce hospital readmission.

Detailed Description

Methods : ICAME is a multicentric, blinded prospective randomized controlled trial. 710 patients originated from 10 centers will be included over a period of 12 months and follow-up for 24 months. All patients have an external evaluation at 6, 12, 18 and 24 months. They were randomized into the usual treatment group (unknown sST2 level) or the interventional treatment group, for whom sST2 level was known at all external consultation and used to guide the treatment. The primary endpoint was the QALY (Quality Adjusted Life Years). The secondary endpoints were the Cost-efficacy ratio, Cost to avoid an hospitalization for heart failure, the readmission rate for any cause at 1 month and at two years, and the evolution of cardiac remodelling determined by the collagene biomarkers.

Registry
clinicaltrials.gov
Start Date
April 27, 2021
End Date
January 1, 2027
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Biomarker guided therapy

Guided therapy using sST-2 monitoring at the discharge from initial hospitalisation, 6, 12, 18 and 24 months of following.

Intervention: Biomarker guided therapy

Outcomes

Primary Outcomes

Cost-utility ratio

Time Frame: 2 years

Cost will be compared between guided therapy using sST-2 levels and usual group. Utility will be derived from the French EQ5D (EuroQol 5 Dimensions), measured at 24 months. QALY (Quality Adjusted Life Years).

Secondary Outcomes

  • Cost-efficacy ratio(2 years)
  • Number of hospitalisation for heart failure(2 years)
  • Cost of initial hospitalisation and rehospitalisation(2 years)

Study Sites (12)

Loading locations...

Similar Trials