University Hospital Zurich
Zurich, 8091, Switzerland
NCT Number: NCT02755298
The study seeks primarily to determine the chronic clinical effect of AZA on exercise capacity (6MWD) compared to placebo.
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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. 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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo) at rest and exercise
Time frame: 5 weeks
actigraphy
Time frame: 5 weeks
measured by echocardiography
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
Time frame: 5 weeks
At the end of both periods (AZA and Placebo)
University of Zurich
Other
Chronic Clinical Effect of Acetazolamide in Pulmonary Hypertension
Acronym: ChronicAZA
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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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