Under construction – not a live service
Sign in

2025-521101-40-00Not yet recruitingPhase 4

GLIFLOFASTER : EARLY GLIFLOZIN TREATMENT IN ELDERLY PATIENT HOSPITALIZED FOR DECOMPENSATED CHRONIC HEART FAILURE ADMITTED IN THE EMERGENCY ROOM - A FEASIBILITY STUDY

Source: EU CTIS (euclinicaltrials.eu) · Last updated 31 Mar 2026

Next steps

Brief summary (registry, in English)

Assess the overall feasibility of a prospective randomized study comparing early initiation of gliflozin treatment with telephone counseling in the emergency department with standard care in elderly patients admitted to the emergency department for decompensated chronic heart failure and not treated with gliflozins.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
144 (estimated)
First submitted
22 Dec 2025
Start date
1 Mar 2026
Lead sponsor
Centre Hospitalier Regional Universitaire
EU CT number
2025-521101-40-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 144
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Presence of acute coronary syndrome on ECG or within 30 days prior to randomization,
  • Percutaneous or surgical coronary intervention planned or performed within 30 days prior to randomization,

Other illness

  • Type 1 diabetes,
  • Any other medical condition that would put the patient at risk or could influence the results of the study,
  • Chronic kidney disease (glomerular filtration rate < 25 ml/min/1.73 m²),
  • Any severe valvular heart disease that may require surgery during the study.
  • Known intolerance or history of hypersensitivity to the active substance or any of the excipients in the medication
  • Persons subject to legal protection measures, psychiatric care, persons admitted to a health or social care facility,

Other

  • Individuals unable to express consent, follow instructions, or comply with follow-up procedures,
  • Not affiliated with or not a beneficiary of a French social security system,
  • Subject is in the exclusion period of another study or listed in the “national volunteer registry.”
  • The patient is finally referred and admitted to the Cardiology Department.
  • The patient is ultimately referred to return home or to a residential care facility for dependent elderly people.
  • Cardiogenic shock,
  • Persons deprived of liberty,

Who the study is looking for

  • Male or female, age ≥ 75 years
  • Admitted to the emergency department for acute decompensated heart failure, diagnosed by the emergency physician based on a range of factors including: (i) Worsening symptoms of chronic heart failure - worsening dyspnea or dyspnea at rest - progressive asthenia - weight gain - worsening of edema/abdominal distension/anasarca (ii) AND objective signs or diagnostic tests consistent with peripheral and/or pulmonary congestion - jugular venous distension - bilateral crackles on pulmonary auscultation - presence of S3 gallop on cardiac auscultation - ascites - hepatomegaly - peripheral edema - radiological and/or ultrasound signs of pulmonary congestion - dilatation of the inferior vena cava (iii) AND elevated natriuretic peptides (BNP or NT-proBNP): a. For patients in sinus rhythm: BNP ≥ 400 pg/mL or NT-proBNP ≥ 1,600 pg/mL b. For patients with atrial fibrillation: BNP ≥ 600 pg/mL or NT-proBNP ≥ 2,400 pg/mL) (iv) AND need for treatment intensification upon admission (increased doses of oral diuretics, addition of a second diuretic, or initiation of intravenous diuretic therapy);
  • Patients considered for hospitalization;
  • No pre-existing treatment with gliflozins (empagliflozin or dapagliflozin);
  • Signed and dated informed consent

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (6)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Regional UniversitaireBesancon CedexFranceNot yet recruiting
Centre Hospitalier De ColmarColmar CedexFranceNot yet recruiting
Centre Hospitalier Universitaire de DijonDijonFranceNot yet recruiting
Centre Hospitalier Universitaire ReimsReims CedexFranceNot yet recruiting
Les Hopitaux Universitaires de StrasbourgStrasbourgFranceNot yet recruiting
Hôpital Nord Franche-ComtéTrévenansFranceNot yet recruiting

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.