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NCT06285760Recruiting

Effect of Acetazolamide on Diuresis and Natriuresis in Patients With Acute Heart Failure (SANDI STUDY)

SANDI STUDY: Effect of Acetazolamide on Diuresis and Natriuresis in Patients With Acute Heart Failure.

Source: ClinicalTrials.gov · Last updated 29 Dec 2025

Brief summary (registry, in English)

The goal of this observational study is to assess the natriuretic effect of intravenous acetazolamide in patients admitted with heart failure and persistent congestion despite treatment with intravenous furosemide and sodium-glucose cotransporter type 2 (iSGLT2) inhibitors. The main question it aims to answer is whether there is a difference in natriuresis 24 hours after acetazolamide association to medical treatment recommended by the guidelines (furosemide and ISGLT2).

Status (registry)
Recruiting
Study type
Observational
Enrollment
64 (estimated)
First submitted
8 Jan 2024
Start date
1 Mar 2024
Primary completion date
31 May 2026
Lead sponsor
Puerta de Hierro University Hospital
NCT number
NCT06285760

What you commit to

  • Study type: Observational
  • Planned participants: 64
  • From 1 Mar 2024 to the primary completion date, 31 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Maintenance treatment with acetazolamide/ Treatment with acetazolamide in the month prior to inclusion in the study.
  • Concurrent diagnosis of acute coronary syndrome.

Other illness

  • Type 1 diabetes mellitus
  • History of congenital heart disease requiring surgical correction.
  • History of cardiac transplantation and/or ventricular assist device.
  • Sulfonamide allergy, liver cirrhosis, renal lithiasis.

Lab values

  • GFR \< 20 ml/min/m2 or renal replacement therapy/ultrafiltration at any time prior to the study.
  • Serum potassium less than 3.5 mEq/L.

Other

  • Systolic blood pressure \<90 mmHg or mean arterial pressure \< 65 mmHg.
  • Anticipated need for intravenous inotropes, vasopressors or nitroprusside during the study.
  • Contraindication to ISGLT2.
  • Anticipated exposure to nephrotoxic agents, such as iodinated contrast during admission.
  • Pregnant or breastfeeding patients.
  • Inability to adequately collect diuresis.
  • Venous pH \<7.30
  • Severe aortic stenosis or obstructive hypertrophic cardiomyopathy.

Who the study is looking for

  • Patients admitted for acute heart failure and ≥ 1 clinical sign of volume overload (edema, ascites, or pleural effusion).
  • NTproBNP levels \>1000 pg/mL or BNP \>250 ng/mL on admission.
  • Under treatment with furosemide and iSGLT2 according to European guidelines and indication of association of another diuretic due to residual congestion data defined by ADVOR SCORE\>1.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Julia González González
Coordinator of this site? Confirm its status
MadridSpainRecruiting

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