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Clinical Trials/NL-OMON51476
NL-OMON51476RecruitingNot Applicable

changed right heart volumes and function following diuretic withdrawal in pulmonary hypertension - Diuretic effect on the right heart

Amsterdam UMC0 sites17 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
17

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • - Diagnosed with idiopathic PAH, hereditary PAH, drug- and toxins induced PAH
  • 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

Exclusion Criteria

  • - 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
  • - 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

Investigators

Sponsor
Amsterdam UMC

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