Venous Congestion Validation study
Not yet recruiting
- Conditions
- Heart Failure, Pulmonary hypertension, right-heart catheterization, echocardiography, MRI, hartfalen, pulmonale hypertensie, rechts kathterisatie, echocardiografie
- Registration Number
- NL-OMON22315
- Lead Sponsor
- MUMC+
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
1. Adult patients (i.e. >18 years of age)
2. Receiving right-heart catheterization for a clinical indication
Exclusion Criteria
1. Contra-indication for MRI or unable to undergo MRI protocol due to physical condition
- Current atrial fibrillation/atrial flutter
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our primary endpoint will be the differences and the correlation between pressures in mmHg measured during right heart catheterization, and MRI measurements of venous congestion parameters (flow pattern and dimension changes of vena cava superior).
- Secondary Outcome Measures
Name Time Method i. The differences and the correlation between pressures in mmHg, measured during right heart catheterization and echocardiographic measurements of CVP (vena cava inferior). Additionally, echocardiographic measurement of vena jugularis interna flow will be included.<br /><br>ii. The differences and the correlation between measurements of echocardiography and MRI.<br /><br>iii. Correlation between NT-proBNP and right-sided intra-cardiac pressures<br>