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Completed

NCT Number: NCT02755298

Chronic Clinical Effect of Acetazolamide

The study seeks primarily to determine the chronic clinical effect of AZA on exercise capacity (6MWD) compared to placebo.

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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. We 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 chronic 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 right heart catheterisation (RHC) for a clinical indication and who are diagnosed with precapillary PH (mean pulmonary arterial pressure (mPAP) ≥25 mmHg, pulmonary wedge pressure (PAWP) ≤15mmHg)
  • Patients have to be in a stable condition, on the same medication for >4 weeks

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. Difference in 6 min walk distance

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

Secondary outcomes

  1. Difference of Quality of Life (QoL) assessed by the physical subscale of the living with pulmonary hypertension questionnaire (MLHF)

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  2. Progressive maximal ramp cardiopulmonary exercise testing

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  3. cerebral and muscle tissue oxygenation

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo) at rest and exercise

  4. daily activity

    Time frame: 5 weeks

    actigraphy

  5. morphological and functional parameters of the heart

    Time frame: 5 weeks

    measured by echocardiography

  6. New York Heart Association functional class

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  7. Short-form medical outcome questionnaire (SF-36)

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  8. Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR)

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  9. N-terminal pro-brain natriuretic Peptide (NT-proBNP)

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  10. mean nocturnal oxygen Saturation during ambulatory sleep studies

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  11. apnea/hypopnea index during ambulatory sleep studies

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  12. Stroop test of cognitive performance

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  13. Trail making test (test of cognitive Performance)

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

  14. 5 point test (test of cognitive Performance)

    Time frame: 5 weeks

    At the end of both periods (AZA and Placebo)

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Registry information

Official study title

Chronic Clinical Effect of Acetazolamide in Pulmonary Hypertension

Acronym: ChronicAZA

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Apr 28, 2016
Registry last updated
Dec 19, 2020

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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