changed right heart volumes and function following diuretic withdrawal in pulmonary hypertensio
- Conditions
- pulmonary hypertensionright heart failure1008220610037454
- Registration Number
- NL-OMON51476
- Lead Sponsor
- Amsterdam UMC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 17
- Diagnosed with idiopathic PAH, hereditary PAH, drug- and toxins induced PAH
or CTEPH,
according to ESC/ERS pulmonary hypertension guidelines
- Minimal dosage of 40mg furosemide or 1mg bumetanide a day
- NYHA classification II
- Age >=18 and <=80 years
- Able to understand and willing to sign the Informed Consent Form
- Pregnant subjects
- Inability to provide informed consent
- Change in PAH specific therapy within 3 months before diuretic withdrawal
- Change in (dose of) any other medication
- Hospitalized for acute decompensation within one year before diuretic
withdrawal
- One or more of the following co-morbidities:, uncontrolled systemic
hypertension (>140/90
mmHg) , renal failure (eGFR <30), recent diagnosis of pulmonary
embolism (within 6 months).
- Contraindication for CMR imaging:
o Claustrophobia
o Implanted cardiac defibrillator or pacemaker
o Cochlear implant
- PH of any cause other than permitted in the entry criteria
- Known history of noncompliance considering therapies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Volumes: Right atrial end reservoir volume, right atrial volume at end active<br /><br>emptying, right atrial volume at end passive emptying, right ventricular end<br /><br>diastolic volume (RVEDV) (ml), right ventricular end systolic volume (RVESV)<br /><br>(ml)<br /><br>Function: Right atrial reservoir volume, right atrial passive emptying volume,<br /><br>right atrial active emptying volume, right ventricular ejection fraction (RVEF)<br /><br>(%)<br /><br>Contractility: right atrial and right ventricular strain, NT-pro BNP levels</p><br>
- Secondary Outcome Measures
Name Time Method <p>Other study parameters: bodyweight, 6-minute walking distance, potassium,<br /><br>sodium, creatinine, stroke volume, flow</p><br>