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Completed

NCT Number: NCT02755259

Acute Hemodynamic Effect of Acetazolamide in Pulmonary Hypertension

To study the acute effect of acetazolamide (AZA) on pulmonary hemodynamics in patients with pulmonary hypertension (PH) undergoing clinically indicated right heart catheterisation (RHC).

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

University Hospital Zurich

Zurich, 8091, Switzerland

About this study

Pulmonary hypertension (PH) of various etiologies causes dyspnea, impairs exercise performance and is associated with reduced quality of life (QoL) and survival. Treatment options include therapy for any underlying causes, pulmonary vasodilator drugs, oxygen and, in selected cases, pulmonary endarterectomy or lung transplantation. Unfortunately, PH specific drugs are expensive, associated with side effects and even combined pharmacological treatment is often not sufficient to achieve clinical benefits. Therefore, novel therapeutic drugs are needed. The investigators have recently demonstrated that sleep related breathing disorders, which are common in PH patients, can be improved by both nocturnal oxygen therapy and acetazolamide (AZA). AZA is a carbonic anhydrase (CA) inhibitor that acts as a respiratory stimulant thereby improving oxygenation and possibly PH. There are even data suggesting that CA-inhibitors have a direct pulmonary vasodilator effect. However, the potential role of AZA in the treatment of PH has not been conclusively studied. Therefore, the purpose of the current project is to investigate, the acute hemodynamic clinical effects of AZA in PH patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients undergoing RHC for a clinical indication and who are diagnosed with precapillary PH (mPAP ≥25 mmHg, pulmonary wedge pressure (PAWP) ≤15mmHg)

Exclusion criteria

  • Patients in whom a RHC is clinically not indicated
  • pregnant women
  • PH in left heart disease or with more than mild chronic obstructive pulmonary disease or restrictive lung disease.

Treatment and study plan

Acetazolamide

Drug

Placebo

Drug

Primary outcomes

  1. Pulmonary vascular resistance (PVR) AZA vs. Placebo (rest)

    Time frame: 60 minutes

    At the end of phase at rest

  2. PVR AZA vs. Placebo (exercise)

    Time frame: 60 minutes

    At the end of phase at exercise

  3. PVR AZA vs. Placebo (hypoxia)

    Time frame: 60 minutes

    At the end of phase under hypoxia

Secondary outcomes

  1. partial pressure of the oxygen

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  2. Oxygen uptake

    Time frame: 15 minutes

  3. minute ventilation

    Time frame: 15 minutes

  4. arterial oxygenation

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  5. tissue oxygenation

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  6. mean pulmonary arterial pressure

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  7. cardiac output

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  8. cardiac index

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  9. pulmonary wedge pressure

    Time frame: 60 minutes

    At the end of each phase (rest, exercise and hypoxia)

  10. Borg scale dyspnea and leg effort

    Time frame: 15 minutes

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Registry information

Acronym: AcuteAZA

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Apr 28, 2016
Registry last updated
Aug 13, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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