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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 (ICAME)

Primary Purpose

Heart Failure

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Biomarker guided therapy
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Heart Failure focused on measuring Heart failure, Biomarker, Guided therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • 18 years or older
  • Hospitalization for heart failure (NTproBNP(N-terminal pro-Brain Natriuretic Peptid) ≥450 pg/ml (ou BNP ≥400 pg/ml)

Exclusion criteria:

  • Waiting for heart transplantation
  • Scheduled valve surgery
  • No fluent french
  • Not able to provide informed consent
  • Hemodynamic instability
  • Poor outcome during the first week.
  • Pregnancy
  • Participating to other study

Sites / Locations

  • Lapeyronie Hospital
  • Arnaud de Villeneuve HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Biomarker guided therapy

Arm Description

Usual management of heart failure. The sST-2 level will be blunted.

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

Outcomes

Primary Outcome Measures

Cost-utility ratio
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 Outcome Measures

Cost-efficacy ratio
Cost to avoid an hospitalisation for heart failure
Cost of initial hospitalisation and rehospitalisation
Including hospitalisation, imaging and biological analysis
Number of hospitalisation for heart failure
Number of hospitalisation for heart failure

Full Information

First Posted
September 14, 2020
Last Updated
December 31, 2021
Sponsor
University Hospital, Montpellier
Collaborators
EURO BIO Scientific
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1. Study Identification

Unique Protocol Identification Number
NCT04554277
Brief Title
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
Acronym
ICAME
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
April 27, 2021 (Actual)
Primary Completion Date
April 2025 (Anticipated)
Study Completion Date
April 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
Collaborators
EURO BIO Scientific

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart failure, Biomarker, Guided therapy

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective
Masking
Participant
Allocation
Randomized
Enrollment
710 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Usual management of heart failure. The sST-2 level will be blunted.
Arm Title
Biomarker guided therapy
Arm Type
Experimental
Arm Description
Guided therapy using sST-2 monitoring at the discharge from initial hospitalisation, 6, 12, 18 and 24 months of following.
Intervention Type
Biological
Intervention Name(s)
Biomarker guided therapy
Intervention Description
Guided therapy using sST-2 monitoring at the discharge from initial hospitalisation, 6, 12, 18 and 24 months of following.
Primary Outcome Measure Information:
Title
Cost-utility ratio
Description
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).
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Cost-efficacy ratio
Description
Cost to avoid an hospitalisation for heart failure
Time Frame
2 years
Title
Cost of initial hospitalisation and rehospitalisation
Description
Including hospitalisation, imaging and biological analysis
Time Frame
2 years
Title
Number of hospitalisation for heart failure
Time Frame
30 days
Title
Number of hospitalisation for heart failure
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: 18 years or older Hospitalization for heart failure (NTproBNP(N-terminal pro-Brain Natriuretic Peptid) ≥450 pg/ml (ou BNP ≥400 pg/ml) Exclusion criteria: Waiting for heart transplantation Scheduled valve surgery No fluent french Not able to provide informed consent Hemodynamic instability Poor outcome during the first week. Pregnancy Participating to other study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Paul CRISTOL, MD, PhD
Phone
(0)4 67 33 83 14
Ext
+33
Email
jp-cristol@chu-montpellier.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Anne-Marie GORCE DUPUY
Phone
(0)4 67 33 79 61
Email
am-dupuy@chu-montpellier.fr
Facility Information:
Facility Name
Lapeyronie Hospital
City
Montpellier
State/Province
Occitanie
ZIP/Postal Code
34295
Country
France
Individual Site Status
Active, not recruiting
Facility Name
Arnaud de Villeneuve Hospital
City
Montpellier
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francois ROUBILLE, MD, phD
Phone
04 67 33 61 82
Ext
+33
Email
f-roubille@chu-montpellier.fr

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The general goal is to make the study data available to interested researchers as well as to provide proof of transparency for the study. Data (and an accompanying data dictionary) will be de-identified and potentially further cleaned or aggregated as the investigators deem necessary to protect participant anonymity. Data will be made available to persons who address a reasonable request to the study director and fulfil the requirements stipulated by the French CNIL (Commission National Informatic Liberty).
IPD Sharing Time Frame
24 months after randomisation

Learn more about this trial

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

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