Clinical Research Directory

Inclusion Criteria: 1. Adults aged 18 years or older who are capable of providing informed consent, or who meet applicable legally authorized representative requirements where permitted. 2. Individuals undergoing routine clinical evaluation, diagnostic imaging, monitoring, treatment, or longitudinal follow-up, including individuals with relevant cardiovascular, vascular, pulmonary, renal, systemic, or other conditions represented within the OMNIPHYS research framework. 3. Healthy volunteers without the conditions under study may participate as reference participants. 4. Ability to undergo at least one protocol-relevant physiologic or imaging assessment and/or contribute eligible routinely collected clinical data. 5. Availability of sufficient clinical, physiologic, imaging, or longitudinal outcome data for the applicable analysis. 6. Willingness to permit collection and longitudinal analysis of protocol-defined research data in accordance with informed consent and applicable privacy and data-governance requirements. Exclusion Criteria: 1. Inability or unwillingness to provide informed consent or otherwise meet applicable consent requirements. 2. Inability to obtain interpretable protocol-relevant physiologic or imaging data when such data are required for the applicable analysis. 3. Conditions or circumstances that, in the judgment of the responsible clinical investigator, make participation inappropriate or prevent meaningful longitudinal follow-up. 4. Withdrawal of consent or request for discontinuation of research participation where applicable. 5. Any circumstance that would prevent collection, secure handling, or analysis of study data in accordance with the approved protocol and applicable requirements.