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NCT05179356CompletedPhase 2

Dapagliflozin in Pulmonary Arterial Hypertension

Effects of DAPAgliflozin on Cardiopulmonary Exercise Capacity and Hemodynamics in Pulmonary Arterial Hypertension: A Double Blind Randomized Trial. (DAPAH-trial)

Source: ClinicalTrials.gov · Last updated 21 Jan 2026

Brief summary (registry, in English)

The purpose of this study is to investigate the effects of dapagliflozin on exercise capacity and hemodynamics in patients with pulmonary arterial hypertension

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
52 (actual)
First submitted
16 Dec 2021
Start date
1 Jan 2023
Primary completion date
13 Jan 2026
Lead sponsor
Mads Ersbøll
NCT number
NCT05179356
EU CT number
2024-518551-37-00
EudraCT number
2021-006787-25

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 52
  • From 1 Jan 2023 to the primary completion date, 13 Jan 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

  • Treatment with an SGLT2i within 6 months prior to baseline
  • Listed for lung transplantation at the time of screening
  • Planned initiation of iv prostacyclin therapy/ IPA or current dose escalation planned

Other illness

  • Known allergy to the study medication
  • Type 1 or type 2 diabetes

Lab values

  • Impaired renal function with an eGFR \< 30 mL/min/m2 within four weeks of screening
  • LVEF \< 50%

Other

  • Severe liver dysfunction (Child-Pugh class c)
  • Planned pulmonary endarterectomy or pulmonary balloon angioplasty.
  • Diagnosis of PAH group 2, 3 or 5

Who the study is looking for

  • A diagnosis of PAH group 4 or group 1 in any of the following subtypes:
    • Idiopathic PAH (iPAH)
    • Heritable PAH (hPAH)
    • Connective tissue disease associated PAH (aPAH)
    • Associated with congenital heart disease (aPAH)
    • In case of PH in group 4, no further invasive treatment including pulmonary endarterectomy or pulmonary balloon angioplasty must be planned at time of inclusion.
  • Symptomatic PAH in WHO functional class II-III as assessed by the screening clinician.
  • Clinically stable patients on pulmonary vasodilator treatment with PDE5i, ERA, PA/IPA alone or in combination without considerations from the treating physician team towards treatment escalation and a treatment duration of at least four weeks. Clinical stability defined as stable symptoms without progression as assessed by treating clinician and without the need for unplanned hospital admissions due to worsening PAH within three months of screening.
  • Fertile women (\< 50 years of age) must use safe contraceptives (Intra uterine device or hormonal contraception) for the duration of the study and have a negative pregnancy test
  • Able to understand the written patient information in Danish and give informed consent.
  • Age ≥ 18 years
  • Ability to perform cardio pulmonary exercise test

Age in the registry: 18 years to - · 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
Rigshospitalet
Coordinator of this site? Confirm its status
Copenhagen OeDenmarkCompleted

Related publications

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