University Hospital Zurich
Zurich, 8091, Switzerland
NCT Number: NCT02755259
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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Notify Me20 year–80 year
All sexes
Interventional
Phase 2 / Phase 3
Zurich, 8091, Switzerland
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 60 minutes
At the end of phase at rest
Time frame: 60 minutes
At the end of phase at exercise
Time frame: 60 minutes
At the end of phase under hypoxia
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 15 minutes
Time frame: 15 minutes
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 60 minutes
At the end of each phase (rest, exercise and hypoxia)
Time frame: 15 minutes
University of Zurich
Other
Acronym: AcuteAZA
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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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