COVID-19NCT05205642
Exercise Fatigue Parameters and Endothelial Function in Pediatric Patients With a History of COVID-19 Infection or MIS-C
A study testing Cardiopulmonary exercise test (CPET), Peripheral Arterial Tonography (PAT) using the EndoPAT™ device and Endothelin in people with COVID-19 and MIS-C Associated With COVID-19, run by Rambam Health Care Campus at 1 site in Israel.
Trial summary
Acute coronavirus disease 2019 (COVID-19) infection can include cardiac and pulmonary manifestations as well as post-infectious complications such as multisystem inflammatory syndrome (MIS-C), also known as pediatric inflammatory multisystem syndrome (PIMS / PIMS-TS). Read more about this study
- Who is it for?
- Ages 5 years and older
- Conditions the study is for
- COVID-19, MIS-C Associated With COVID-19
- What is being tested?
- Cardiopulmonary exercise test (CPET), Peripheral Arterial Tonography (PAT) using the EndoPAT™ device and Endothelin
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteIsrael
- Study dates
- 1 Nov 2021to 30 Jun 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 5 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Patients aged 5 years and older recovering from COVID-19 infection.
- For EndoPAT assessment-at least 3 months since the patient was diagnosed with COVID -19 infection or with PIMS
Who cannot join
- Cardiac or pulmonary comorbidity other than COVID-19 related morbidity.
- Inability to perform all study assessments. If a patient will be able to complete one of the assessments or more, the data will be collected and included in the analysis.
- Intercurrent systemic conditions or illness and/or medication use that could affect cardiopulmonary exercise capacity or EndoPAT™.
Trial locations and contacts
1 site in 1 country.
Israel1 site, 1 recruiting
- Recruiting
Rambam Medical Center
Haifa
Ronen Bar-Yoseph, MD, +972-4-7774360, r_bar-yoseph@rambam.health.gov.il
Merav Zucker-Toledano, MD, +972-4-7774630, M_ZUCKER@rambam.health.gov.il
About this study
Official title: The Evaluation of Exercise Fatigue Parameters and Endothelial Function in Pediatric Patients With a History of COVID-19 Infection or Multisystem Inflammatory Syndrome (MIS-C)
Acute coronavirus disease 2019 (COVID-19) infection can include cardiac and pulmonary manifestations as well as post-infectious complications such as multisystem inflammatory syndrome (MIS-C), also known as pediatric inflammatory multisystem syndrome (PIMS / PIMS-TS). The precise etiology for COVID-19 symptoms and MIS-C is still obscure but there is evidence that endothelial damage may play a role. At recovery, symptoms such as dyspnea, fatigue, weakness, myalgia, chest pain and palpitations are prevalent. Data regarding functional capacity, cardiopulmonary and vascular function post COVID-19 infection are scarce. To the best of our knowledge, few studies has evaluated functional capacity of patients recovering from COVID-19 infection and complications using cardiopulmonary exercise testing (CPET), and no study included endothelial function assessment.
Aims I. To investigate the effect of COVID-19 infection on cardiovascular and pulmonary function and exercise parameters in the pediatric and adult population.
Read more
II. To investigate the effect of PIMS on endothelial function in pediatric population.
Research hypothesis:
- After COVID-19 infection, aerobic function is impaired due to cardiac and/or pulmonary limitation
- Endothelial function in children after PIMS is impaired in comparison to healthy individuals and to patients after COVID infection with mild symptoms.
Importance of the study: Cardiovascular and pulmonary assessment of patients recovering from COVID-19 infection using CPET and Peripheral Arterial Tonography (EndoPAT™) has not been reported previously, and will provide new insights into the long term significance of COVID-19 infection.
Read the detailed description
Introduction: coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 is currently a major public health challenge. COVID-19 infection results in diverse symptoms and morbidity. In severe cases, COVID-19 pathophysiology includes destruction of lung epithelial cells, thrombosis, and vascular leak leading to acute respiratory distress syndrome (ARDS) and subsequent pulmonary fibrosis. Clinical manifestations of COVID-19 can include cardiac involvement with complications, such as myocarditis (including fulminant cases), arrhythmias and rapid-onset heart failure. In children, severe acute infection is less common than in adults. Another COVID-19 related entity is a delayed life-threatening syndrome mimicking incomplete Kawasaki disease (KD) and toxic shock syndrome now designated as pediatric inflammatory multisystem syndrome (PIMS-TS) or MIS-C. Although rare, this syndrome remains an important source of pediatric COVID-19 related morbidity and mortality. The cardiovascular system is one of the major systems affected by this syndrome, manifesting mainly as myocarditis and/or coronary vasculitis. Endothelial dysfunction (ED) is a frequent long-term complication in patients after KD, manifesting as diminished production or availability of nitric oxide (NO) and an imbalance in the relative contribution of endothelium-derived relaxing and contracting factors. Little is known regarding ED post COVID-19 in the pediatric population but there is some evidence that endothelial injury might play a role in the pathogenesis of the disease. Patients who recover from acute COVID-19 infection or post-COVID-19 syndrome can have diverse complaints and symptoms such as chest pain, palpitations, weakness, myalgia and dyspnea. Several "return to play" guidelines exist for athletes, adults and children, due to concerns about long term cardiovascular and respiratory complications. Cardiopulmonary exercise testing (CPET) has become an important clinical tool to evaluate exercise capacity and predict outcome in patients with heart failure and other cardiac conditions. It provides assessment of integrative exercise responses involving the pulmonary, cardiovascular, and skeletal muscle systems, which are not adequately reflected through the measurement of individual organ system function. CPET is increasingly being used in a wide spectrum of clinical applications for evaluation of undiagnosed exercise intolerance and for objective determination of functional capacity and impairment. Few reports are available regarding CPET in post- COVID -19 infection adult patients, most of them after severe acute illness. Those reports demonstrated decreased aerobic capacity, not related to pulmonary limitation.
Peripheral Arterial Tonography (EndoPAT™) is a non-invasive and operator independent assessment of endothelial dysfunction. It evaluates the change in the volume of the pulse, using a volume sensor that is placed on the second fingertip both on the hand that is under evaluation and the free hand, measuring the reactive hyperemia mediated by NO release in response to local ischemia. EndoPAT™ has been in clinical research use for evaluation of endothelial changes in vasculitis, and has been deemed feasible and reproducible in the pediatric population. EndoPAT™, has been validated as a good evaluation tool for various blood-vessel related functions including arterial stiffness. In children, EndoPAT™ feasibility has been demonstrated in various conditions including inflammatory bowel disease (IBD) and Type I diabetes mellitus. We will therefore use this method to evaluate possible endothelial dysfunction in patients who suffered from PIMS. Endothelial dysfunction was previously evaluated by serum levels of endothelin, endothelin is a vasoconstricting substances that was previously used to evaluate endothelial dysfunction and high levels of endothelin were previously proved to be associated with coronary vasoconstriction. We aim to evaluate children, adolescents and adults, who had infection with COVID-19 or were diagnosed with PIMS and compare them to healthy controls, using pulmonary function tests, echocardiography, 6-min walk test (6MWT), CPET ,EndoPAT™ and serum levels of endothelin in order to identify long term cardiac or pulmonary residual function/limitation which might explain the symptoms or the long-term cardiopulmonary sequela of COVID-19 infection. Study design: Pediatric and adult patients recovering from COVID-19 with or without complaints or followed at the PIMS outpatient clinic or referred to the CPET clinic at Rambam Medical Center will be enrolled in the study. Data will be collected retrospectively/ prospectively, approximately 3 months after acute infection or post- COVID PIMS. CPET will be performed as part of the clinical evaluation recommended by the following physician. EndoPAT assesment- as part of the research. and blood endothelin levels- as part of the research. Participants will undergo all or part of the evaluation, and possibly repeated evaluations if needed. For CPET results each patient will be age- and sex-matched with an historical control from our CPET research database containing records of 200 healthy patients. For EndoPAT results- patient recovering from COVID-19 without PIMS will be evaluated as controls and the data will be compared to normal known values for age.
- Conditions
- COVID-19, MIS-C Associated With COVID-19
- Being tested
- Cardiopulmonary exercise test (CPET), Peripheral Arterial Tonography (PAT) using the EndoPAT™ device, Endothelin
- Keywords
- Cardiopulmonary Exercise Testing, EndoPAT, COVID-19
- Medical subject headings
- COVID-19, pediatric multisystem inflammatory disease, COVID-19 related
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cardiopulmonary exercise test (CPET)Device
Cardiopulmonary exercise testing (CPET) using a Quark CPET metabolic cart (Rome, Italy) according to American Thoracic Society (ATS) guidelines. A symptom-limited test on a treadmill will be performed, using incremental ramp Bruce protocol up to exhaustion. Patients who will not be able to perform the test on a treadmill will be tested on a cycle ergometer beginning with a no-resistance warm-up lasting 2-3 minutes, followed by incrementing resistance (8-30 Watts/minute) adapted to the patient's functional capacities according to the examiner's free judgment, up to exhaustion.
Peripheral Arterial Tonography (PAT) using the EndoPAT™ deviceDevice
A volume sensor measuring reactive hyperemia is placed on the second fingertip of both hands. First the device evaluates the baseline volume of the pulse. Then, we will apply pressure that is 50 mmHg higher than the baseline systolic pressure of the examinee on the evaluated hand for five minutes, using a sphygmomanometer cuff. After the pressure is released on the evaluated hand, the new pulse volume is tested. To neutralize the effects of the autonomous systemic response, the program divides the difference of the pulse volume in the examined hand by the difference in the untested hand and we get the Reactive Hyperemic Index (RHI) which represents the endothelial function in the tested hand. During the examination, the calculated arterial tonometry graph is generated, and out of it the RHI will be automatically calculated, using the EndoPAT2000™ program.
EndothelinDiagnostic test
For Endothelin levels we will use the Endothelin ELISA kit from R\&D company, and for measurement 1 cc of serum will be needed.
| Study group | Role | What they receive |
|---|---|---|
| Patients recovering from COVID-19 | Experimental | Pediatric and adult patients recovering from COVID-19 with or without complaints. Receives: Device: Cardiopulmonary exercise test (CPET); Device: Peripheral Arterial Tonography (PAT) using the EndoPAT™ device; Diagnostic Test: Endothelin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Exercise capacity
Oxygen uptake evaluated by cardiopulmonary exercise testing (CPET)
Measured: Measured continuously during 15 minutes of the exercise test (CPET)
Secondary outcomes (3)
Six minute walk test (6MWT)
patients will be instructed to walk as far as possible for six minutes in a 30-meter long enclosed corridor with a flat and hard surface, marked at every meter. Meters will be calculated at the end of the test.
Measured: Six minutes
Endothelin level
One ml of serum will be needed using the Endothelin ELISA kit from R\&D company.
Measured: Five minutes for the blood to be drawn.
Echocardiography
Cardiac assessment using echocardiography for anatomical and functional evaluation.
Measured: Ten minutes.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Jan 2022
- Study start1 Nov 2021
- Primary completion31 Dec 2023 (estimated)
- Study completion30 Jun 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for COVID-19Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Rambam Health Care Campus
- Sponsor type
- University, hospital or other
- Collaborators
- The Baruch Padeh Medical Center, Poriya
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05205642
- Sponsor's protocol ID
- 0768-20-RMB
- Status last verified
- Jan 2022
- First submitted
- 23 Jan 2022
- Last updated
- 25 Jan 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 25 Jan 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Evaluation of Exercise Fatigue Parameters and Endothelial Function in Pediatric Patients With a History of COVID-19 Infection or Multisystem Inflammatory Syndrome (MIS-C)
- ClinicalTrials.gov ID
- NCT05205642
- Acronym / sponsor ID
- 0768-20-RMB
- Conditions
- COVID-19, MIS-C Associated With COVID-19
- Keywords
- Cardiopulmonary Exercise Testing, EndoPAT, COVID-19
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Rambam Health Care CampusUniversity, hospital or other
- Collaborators
- The Baruch Padeh Medical Center, Poriya
- Study start
- 1 Nov 2021 (actual)
- Primary completion
- 31 Dec 2023 (estimated)
- Study completion
- 30 Jun 2024 (estimated)
- First posted
- 25 Jan 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Acute coronavirus disease 2019 (COVID-19) infection can include cardiac and pulmonary manifestations as well as post-infectious complications such as multisystem inflammatory syndrome (MIS-C), also known as pediatric inflammatory multisystem syndrome (PIMS / PIMS-TS). The precise etiology for COVID-19 symptoms and MIS-C is still obscure but there is evidence that endothelial damage may play a role. At recovery, symptoms such as dyspnea, fatigue, weakness, myalgia, chest pain and palpitations are prevalent. Data regarding functional capacity, cardiopulmonary and vascular function post COVID-19 infection are scarce. To the best of our knowledge, few studies has evaluated functional capacity of patients recovering from COVID-19 infection and complications using cardiopulmonary exercise testing (CPET), and no study included endothelial function assessment.
Aims I. To investigate the effect of COVID-19 infection on cardiovascular and pulmonary function and exercise parameters in the pediatric and adult population.
II. To investigate the effect of PIMS on endothelial function in pediatric population.
Research hypothesis:
- After COVID-19 infection, aerobic function is impaired due to cardiac and/or pulmonary limitation
- Endothelial function in children after PIMS is impaired in comparison to healthy individuals and to patients after COVID infection with mild symptoms.
Importance of the study: Cardiovascular and pulmonary assessment of patients recovering from COVID-19 infection using CPET and Peripheral Arterial Tonography (EndoPAT™) has not been reported previously, and will provide new insights into the long term significance of COVID-19 infection.
Detailed description
Introduction: coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 is currently a major public health challenge. COVID-19 infection results in diverse symptoms and morbidity. In severe cases, COVID-19 pathophysiology includes destruction of lung epithelial cells, thrombosis, and vascular leak leading to acute respiratory distress syndrome (ARDS) and subsequent pulmonary fibrosis. Clinical manifestations of COVID-19 can include cardiac involvement with complications, such as myocarditis (including fulminant cases), arrhythmias and rapid-onset heart failure. In children, severe acute infection is less common than in adults. Another COVID-19 related entity is a delayed life-threatening syndrome mimicking incomplete Kawasaki disease (KD) and toxic shock syndrome now designated as pediatric inflammatory multisystem syndrome (PIMS-TS) or MIS-C. Although rare, this syndrome remains an important source of pediatric COVID-19 related morbidity and mortality. The cardiovascular system is one of the major systems affected by this syndrome, manifesting mainly as myocarditis and/or coronary vasculitis. Endothelial dysfunction (ED) is a frequent long-term complication in patients after KD, manifesting as diminished production or availability of nitric oxide (NO) and an imbalance in the relative contribution of endothelium-derived relaxing and contracting factors. Little is known regarding ED post COVID-19 in the pediatric population but there is some evidence that endothelial injury might play a role in the pathogenesis of the disease. Patients who recover from acute COVID-19 infection or post-COVID-19 syndrome can have diverse complaints and symptoms such as chest pain, palpitations, weakness, myalgia and dyspnea. Several "return to play" guidelines exist for athletes, adults and children, due to concerns about long term cardiovascular and respiratory complications. Cardiopulmonary exercise testing (CPET) has become an important clinical tool to evaluate exercise capacity and predict outcome in patients with heart failure and other cardiac conditions. It provides assessment of integrative exercise responses involving the pulmonary, cardiovascular, and skeletal muscle systems, which are not adequately reflected through the measurement of individual organ system function. CPET is increasingly being used in a wide spectrum of clinical applications for evaluation of undiagnosed exercise intolerance and for objective determination of functional capacity and impairment. Few reports are available regarding CPET in post- COVID -19 infection adult patients, most of them after severe acute illness. Those reports demonstrated decreased aerobic capacity, not related to pulmonary limitation.
Peripheral Arterial Tonography (EndoPAT™) is a non-invasive and operator independent assessment of endothelial dysfunction. It evaluates the change in the volume of the pulse, using a volume sensor that is placed on the second fingertip both on the hand that is under evaluation and the free hand, measuring the reactive hyperemia mediated by NO release in response to local ischemia. EndoPAT™ has been in clinical research use for evaluation of endothelial changes in vasculitis, and has been deemed feasible and reproducible in the pediatric population. EndoPAT™, has been validated as a good evaluation tool for various blood-vessel related functions including arterial stiffness. In children, EndoPAT™ feasibility has been demonstrated in various conditions including inflammatory bowel disease (IBD) and Type I diabetes mellitus. We will therefore use this method to evaluate possible endothelial dysfunction in patients who suffered from PIMS. Endothelial dysfunction was previously evaluated by serum levels of endothelin, endothelin is a vasoconstricting substances that was previously used to evaluate endothelial dysfunction and high levels of endothelin were previously proved to be associated with coronary vasoconstriction. We aim to evaluate children, adolescents and adults, who had infection with COVID-19 or were diagnosed with PIMS and compare them to healthy controls, using pulmonary function tests, echocardiography, 6-min walk test (6MWT), CPET ,EndoPAT™ and serum levels of endothelin in order to identify long term cardiac or pulmonary residual function/limitation which might explain the symptoms or the long-term cardiopulmonary sequela of COVID-19 infection. Study design: Pediatric and adult patients recovering from COVID-19 with or without complaints or followed at the PIMS outpatient clinic or referred to the CPET clinic at Rambam Medical Center will be enrolled in the study. Data will be collected retrospectively/ prospectively, approximately 3 months after acute infection or post- COVID PIMS. CPET will be performed as part of the clinical evaluation recommended by the following physician. EndoPAT assesment- as part of the research. and blood endothelin levels- as part of the research. Participants will undergo all or part of the evaluation, and possibly repeated evaluations if needed. For CPET results each patient will be age- and sex-matched with an historical control from our CPET research database containing records of 200 healthy patients. For EndoPAT results- patient recovering from COVID-19 without PIMS will be evaluated as controls and the data will be compared to normal known values for age.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients recovering from COVID-19 | Experimental | Device: Cardiopulmonary exercise test (CPET), Device: Peripheral Arterial Tonography (PAT) using the EndoPAT™ device, Diagnostic Test: EndothelinPediatric and adult patients recovering from COVID-19 with or without complaints. |
Who may qualify
- Ages
- 5 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (2 listed)
- Patients aged 5 years and older recovering from COVID-19 infection.
- For EndoPAT assessment-at least 3 months since the patient was diagnosed with COVID -19 infection or with PIMS
Key exclusion criteria (3 listed)
- Cardiac or pulmonary comorbidity other than COVID-19 related morbidity.
- Inability to perform all study assessments. If a patient will be able to complete one of the assessments or more, the data will be collected and included in the analysis.
- Intercurrent systemic conditions or illness and/or medication use that could affect cardiopulmonary exercise capacity or EndoPAT™.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cardiopulmonary exercise test (CPET)Cardiopulmonary exercise testing (CPET) using a Quark CPET metabolic cart (Rome, Italy) according to American Thoracic Society (ATS) guidelines. A symptom-limited test on a treadmill will be performed, using incremental ramp Bruce protocol up to exhaustion. Patients who will not be able to perform the test on a treadmill will be tested on a cycle ergometer beginning with a no-resistance warm-up lasting 2-3 minutes, followed by incrementing resistance (8-30 Watts/minute) adapted to the patient's functional capacities according to the examiner's free judgment, up to exhaustion. | Device | Patients recovering from COVID-19 |
| Peripheral Arterial Tonography (PAT) using the EndoPAT™ deviceA volume sensor measuring reactive hyperemia is placed on the second fingertip of both hands. First the device evaluates the baseline volume of the pulse. Then, we will apply pressure that is 50 mmHg higher than the baseline systolic pressure of the examinee on the evaluated hand for five minutes, using a sphygmomanometer cuff. After the pressure is released on the evaluated hand, the new pulse volume is tested. To neutralize the effects of the autonomous systemic response, the program divides the difference of the pulse volume in the examined hand by the difference in the untested hand and we get the Reactive Hyperemic Index (RHI) which represents the endothelial function in the tested hand. During the examination, the calculated arterial tonometry graph is generated, and out of it the RHI will be automatically calculated, using the EndoPAT2000™ program. | Device | Patients recovering from COVID-19 |
| EndothelinFor Endothelin levels we will use the Endothelin ELISA kit from R\&D company, and for measurement 1 cc of serum will be needed. | Diagnostic test | Patients recovering from COVID-19 |
Primary outcome
Exercise capacity
Time frame: Measured continuously during 15 minutes of the exercise test (CPET)
Oxygen uptake evaluated by cardiopulmonary exercise testing (CPET)
3 secondary outcomes
Six minute walk test (6MWT)
Time frame: Six minutes
Endothelin level
Time frame: Five minutes for the blood to be drawn.
Echocardiography
Time frame: Ten minutes.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Jan 2022.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Cardiopulmonary exercise test (CPET), Peripheral Arterial Tonography (PAT) using the EndoPAT™ device and Endothelin in people with COVID-19 and MIS-C Associated With COVID-19, run by Rambam Health Care Campus at 1 site in Israel.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 25 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Ronen Bar-Yoseph, MD (+972-4-777-4360, r_bar-yoseph@rambam.health.gov.il), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Exercise capacity (time frame: Measured continuously during 15 minutes of the exercise test (CPET)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Jan 2022.