Recruiting NCT05849025
A Study of Invasive Hemodynamic for MACHD Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Healthy, Congenital Heart Disease. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Invasive Hemodynamic Control Cohort for The Mayo Clinic Adult Congenital Heart Disease (MACHD) Registry
Overview
This research study is being done to provide comparative data to the Mayo Clinic Adult Congenital Heart Disease Registry.
Primary outcome measures
- Pulmonary vascular reserve [Time frame: Baseline]
Eligibility criteria
Inclusion criteria
- Capacity to Consent
- BMI </= 30
- Systolic BP </= 140mmHg
- Diastolic BP </= 90
- eGFR > 30 (within prior 3 months) to confirm kidney function
- Able to undergo an MRI
Exclusion criteria
- History of Cardiovascular disease that may affect the results of the testing performed.
- Any Current orthopedic limitations
- Currently taking any cardiac medication
- Pregnancy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Mayo Clinic Rochester — Rochester
Identifiers
NCT: NCT05849025 · 23-001939 · R01HL160761