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Chronic Clinical Effect of Acetazolamide (ChronicAZA)

Primary Purpose

Hypertension, Pulmonary

Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Acetazolamide
Placebo
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension, Pulmonary focused on measuring Treatment Outcome, Acetazolamide

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University Hospital Zurich

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Acetazolamide

Placebo

Arm Description

Twice a day 250 mg acetazolamide for 5 weeks

Placebo capsule 250 mg (Mannitol) twice a day 5 weeks

Outcomes

Primary Outcome Measures

Difference in 6 min walk distance
At the end of both periods (AZA and Placebo)

Secondary Outcome Measures

Difference of Quality of Life (QoL) assessed by the physical subscale of the living with pulmonary hypertension questionnaire (MLHF)
At the end of both periods (AZA and Placebo)
Progressive maximal ramp cardiopulmonary exercise testing
At the end of both periods (AZA and Placebo)
cerebral and muscle tissue oxygenation
At the end of both periods (AZA and Placebo) at rest and exercise
daily activity
actigraphy
morphological and functional parameters of the heart
measured by echocardiography
New York Heart Association functional class
At the end of both periods (AZA and Placebo)
Short-form medical outcome questionnaire (SF-36)
At the end of both periods (AZA and Placebo)
Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR)
At the end of both periods (AZA and Placebo)
N-terminal pro-brain natriuretic Peptide (NT-proBNP)
At the end of both periods (AZA and Placebo)
mean nocturnal oxygen Saturation during ambulatory sleep studies
At the end of both periods (AZA and Placebo)
apnea/hypopnea index during ambulatory sleep studies
At the end of both periods (AZA and Placebo)
Stroop test of cognitive performance
At the end of both periods (AZA and Placebo)
Trail making test (test of cognitive Performance)
At the end of both periods (AZA and Placebo)
5 point test (test of cognitive Performance)
At the end of both periods (AZA and Placebo)

Full Information

First Posted
March 24, 2016
Last Updated
December 17, 2020
Sponsor
University of Zurich
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1. Study Identification

Unique Protocol Identification Number
NCT02755298
Brief Title
Chronic Clinical Effect of Acetazolamide
Acronym
ChronicAZA
Official Title
Chronic Clinical Effect of Acetazolamide in Pulmonary Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
October 2016 (undefined)
Primary Completion Date
November 2020 (Actual)
Study Completion Date
November 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Pulmonary
Keywords
Treatment Outcome, Acetazolamide

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Acetazolamide
Arm Type
Experimental
Arm Description
Twice a day 250 mg acetazolamide for 5 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo capsule 250 mg (Mannitol) twice a day 5 weeks
Intervention Type
Drug
Intervention Name(s)
Acetazolamide
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Difference in 6 min walk distance
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
Difference of Quality of Life (QoL) assessed by the physical subscale of the living with pulmonary hypertension questionnaire (MLHF)
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
Progressive maximal ramp cardiopulmonary exercise testing
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
cerebral and muscle tissue oxygenation
Description
At the end of both periods (AZA and Placebo) at rest and exercise
Time Frame
5 weeks
Title
daily activity
Description
actigraphy
Time Frame
5 weeks
Title
morphological and functional parameters of the heart
Description
measured by echocardiography
Time Frame
5 weeks
Title
New York Heart Association functional class
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
Short-form medical outcome questionnaire (SF-36)
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR)
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
N-terminal pro-brain natriuretic Peptide (NT-proBNP)
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
mean nocturnal oxygen Saturation during ambulatory sleep studies
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
apnea/hypopnea index during ambulatory sleep studies
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
Stroop test of cognitive performance
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
Trail making test (test of cognitive Performance)
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks
Title
5 point test (test of cognitive Performance)
Description
At the end of both periods (AZA and Placebo)
Time Frame
5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Silvia Ulrich, MD
Organizational Affiliation
UniversityHospital Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Chronic Clinical Effect of Acetazolamide

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