TACTIC-HF: Sequential Diuretic Strategies in Ambulatory Worsening Heart Failure
TACTIC-HF
TACTIC-HF: Thiazide or Acetazolamide Combination Versus Intravenous Furosemide in Ambulatory Worsening Heart Failure - a Randomized Crossover Trial
2 other identifiers
interventional
60
0 countries
N/A
Brief Summary
TACTIC-HF is a prospective randomized crossover trial designed to compare three ambulatory diuretic strategies in patients with worsening heart failure treated in a specialized heart failure day-hospital program. Participants will receive sequential treatment with:
- 1.intravenous furosemide alone,
- 2.intravenous furosemide combined with oral acetazolamide, and
- 3.intravenous furosemide combined with oral hydrochlorothiazide.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_4
Started Jun 2026
Shorter than P25 for phase_4
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 11, 2026
CompletedFirst Posted
Study publicly available on registry
May 18, 2026
CompletedStudy Start
First participant enrolled
June 15, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2027
Study Completion
Last participant's last visit for all outcomes
January 15, 2027
May 18, 2026
May 1, 2026
7 months
May 11, 2026
May 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Total Urinary Sodium Excretion at 6 Hours
Total urine volume collected during the outpatient treatment session
6 hours
Study Arms (3)
Intravenous Furosemide
ACTIVE COMPARATORParticipants receive outpatient intravenous furosemide according to the study protocol during a structured ambulatory treatment session.
Intravenous Furosemide + Acetazolamide
EXPERIMENTALParticipants receive outpatient intravenous furosemide combined with oral acetazolamide during a structured ambulatory treatment session
Intravenous Furosemide + Hydrochlorothiazide
EXPERIMENTALParticipants receive outpatient intravenous furosemide combined with oral hydrochlorothiazide during a structured ambulatory treatment session
Interventions
Intravenous loop diuretic therapy administered during outpatient treatment sessions according to protocol-defined dosing categories.
Oral acetazolamide administered prior to intravenous loop diuretic therapy during outpatient treatment sessions
Oral hydrochlorothiazide administered prior to intravenous loop diuretic therapy during outpatient treatment sessions.
Eligibility Criteria
You may qualify if:
- Age ≥18 years Chronic heart failure diagnosis according to current guideline definitions Ambulatory worsening heart failure requiring intravenous diuretic therapy in a specialized outpatient setting Evidence of clinical or objective congestion Chronic outpatient loop diuretic therapy Ability to comply with study procedures Written informed consent
You may not qualify if:
- Hemodynamic instability or cardiogenic shock Requirement for immediate hospitalization Acute coronary syndrome, active infection, pulmonary embolism, or uncontrolled arrhythmia Severe electrolyte abnormalities Advanced renal failure requiring dialysis Pregnancy or breastfeeding Contraindication or allergy to study medications Current treatment with acetazolamide or thiazide diuretics Any condition that, in the opinion of the investigators, would make study participation unsafe or interfere with study procedures
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
Abbo AR, Gruber A, Volis I, Aronson D, Girerd N, Lund Kristensen S, Zukermann R, Alberkant N, Sitnitsky E, Kruger A, Khasis P, Bravo E, Elad B, Helmer Levin L, Caspi O. Diuresis Efficacy in Ambulatory Congested Heart Failure Patients: Intrapatient Comparison of 3 Diuretic Regimens (DEA-HF). JACC Heart Fail. 2024 Aug;12(8):1396-1405. doi: 10.1016/j.jchf.2024.04.014. Epub 2024 May 11.
PMID: 38739124BACKGROUNDTrullas JC, Morales-Rull JL, Casado J, Carrera-Izquierdo M, Sanchez-Marteles M, Conde-Martel A, Davila-Ramos MF, Llacer P, Salamanca-Bautista P, Perez-Silvestre J, Plasin MA, Cerqueiro JM, Gil P, Formiga F, Manzano L; CLOROTIC trial investigators. Combining loop with thiazide diuretics for decompensated heart failure: the CLOROTIC trial. Eur Heart J. 2023 Feb 1;44(5):411-421. doi: 10.1093/eurheartj/ehac689.
PMID: 36423214BACKGROUNDMullens W, Dauw J, Martens P, Verbrugge FH, Nijst P, Meekers E, Tartaglia K, Chenot F, Moubayed S, Dierckx R, Blouard P, Troisfontaines P, Derthoo D, Smolders W, Bruckers L, Droogne W, Ter Maaten JM, Damman K, Lassus J, Mebazaa A, Filippatos G, Ruschitzka F, Dupont M; ADVOR Study Group. Acetazolamide in Acute Decompensated Heart Failure with Volume Overload. N Engl J Med. 2022 Sep 29;387(13):1185-1195. doi: 10.1056/NEJMoa2203094. Epub 2022 Aug 27.
PMID: 36027559BACKGROUND
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
May 11, 2026
First Posted
May 18, 2026
Study Start (Estimated)
June 15, 2026
Primary Completion (Estimated)
January 15, 2027
Study Completion (Estimated)
January 15, 2027
Last Updated
May 18, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share