NCT07593612

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. 1.intravenous furosemide alone,
  2. 2.intravenous furosemide combined with oral acetazolamide, and
  3. 3.intravenous furosemide combined with oral hydrochlorothiazide.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for phase_4

Timeline
7mo left

Started Jun 2026

Shorter than P25 for phase_4

Status
not yet recruiting

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

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 18, 2026

Completed
28 days until next milestone

Study Start

First participant enrolled

June 15, 2026

Expected
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2027

Last Updated

May 18, 2026

Status Verified

May 1, 2026

Enrollment Period

7 months

First QC Date

May 11, 2026

Last Update Submit

May 11, 2026

Conditions

Keywords

worsening heart failure

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 COMPARATOR

Participants receive outpatient intravenous furosemide according to the study protocol during a structured ambulatory treatment session.

Drug: Intravenous furosemide bolus injections

Intravenous Furosemide + Acetazolamide

EXPERIMENTAL

Participants receive outpatient intravenous furosemide combined with oral acetazolamide during a structured ambulatory treatment session

Drug: Intravenous furosemide bolus injectionsDrug: ACETAZOLAMIDE oral capsule

Intravenous Furosemide + Hydrochlorothiazide

EXPERIMENTAL

Participants receive outpatient intravenous furosemide combined with oral hydrochlorothiazide during a structured ambulatory treatment session

Drug: Intravenous furosemide bolus injectionsDrug: Hydrochlorothiazide (HCT)

Interventions

Intravenous loop diuretic therapy administered during outpatient treatment sessions according to protocol-defined dosing categories.

Intravenous FurosemideIntravenous Furosemide + AcetazolamideIntravenous Furosemide + Hydrochlorothiazide

Oral acetazolamide administered prior to intravenous loop diuretic therapy during outpatient treatment sessions

Intravenous Furosemide + Acetazolamide

Oral hydrochlorothiazide administered prior to intravenous loop diuretic therapy during outpatient treatment sessions.

Intravenous Furosemide + Hydrochlorothiazide

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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: 38739124BACKGROUND
  • Trullas 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: 36423214BACKGROUND
  • Mullens 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

AcetazolamideHydrochlorothiazide

Intervention Hierarchy (Ancestors)

ThiadiazolesThiazolesSulfur CompoundsOrganic ChemicalsAzolesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsChlorothiazideBenzothiadiazinesSulfonamidesSulfonesThiazidesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Central Study Contacts

Lucrecia Maria Burgos, MD

CONTACT

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