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DUAL-REGISTERED PROTOCOL // OSF PRE-REGISTERED (DOI: 10.17605/OSF.IO/VPS9D) · CLINICALTRIALS.GOV PRS IN PROGRESS · PROTOCOL ID: DS-CLIN-2026-CARDIO-RESOLVE · PLANNED N = 10,000

CARDIO-RESOLVE™ Registry.
Precision cardiology meets autonomic resilience.

From monogenic channelopathies to the exploding pandemic of post-viral dysautonomia and POTS, traditional cardiology relies on fragmented snapshot testing. CARDIO-RESOLVE™ is a prospective decentralized clinical registry ($N=10,000$) uniting advanced lipidomics, continuous autonomic hemodynamics, and cardiac ion channel genomics under the DeepSensi Cognitive Engine. Participation in the clinical registry is 100% Free.

A tilt-table test in a bright autonomic function laboratory: a patient secured on the tilted table with blood-pressure cuff and ECG leads, a technician adjusting the angle. Clean white…

RESOLVE in the United States: in preparation (IRB submission in preparation, the first country to open).

N = 10,000
cardiology & POTS cohort
POTS & HCM
autonomic & structural focus
Lp(a) & hs-cTnI
high-sensitivity markers
100% Free
clinical registry participation

Registry Strata

Three Specialized Cardiovascular Cohorts

Wide view of a tilt-test laboratory: the patient on the tilt table on the left with a technician at her side; on the right a cardiologist stands at a monitor following heart-rate and…
Cohort 1 · N = 4,000

Postural Orthostatic Tachycardia (POTS) & Dysautonomia

Post-viral autonomic dysfunction, orthostatic intolerance, and small-fiber neuropathy. Serial tracking of supine/standing plasma catecholamines (norepinephrine, epinephrine), renin-aldosterone ratio, and autonomic heart-rate variability under DSS-001.

Cohort 2 · N = 3,000

Hereditary Cardiomyopathies (HCM, DCM, ARVC)

Sarcomeric and structural genetic variants (*TTN, MYBPC3, MYH7, LMNA*). Modeling subclinical myocardial strain, serial high-sensitivity troponin (hs-cTnI), and NT-proBNP kinetic progression curves.

Cohort 3 · N = 3,000

Primary Channelopathies & Refractory Dyslipidemia

Long QT Syndrome (*KCNQ1, KCNH2, SCN5A*), Brugada Syndrome, and Familial Hypercholesterolemia (FH). Advanced particle lipidomics (Lp(a), ApoB, LDL-P) and ion-channel drug safety tensors.

Biomarkers & Outcomes

Hemodynamic & Molecular Primary Endpoints

A family at a bright dining table at home with medical documents spread out and an open laptop showing an abstract, friendly summary layout. Calm, attentive, nobody looks at the camera.
Primary Outcome 1

Orthostatic Tolerance & COMPASS-31

Documented stabilization of orthostatic heart-rate delta and statistically significant reduction in autonomic symptom burden on the COMPASS-31 and Orthostatic Hypotension Questionnaire (OHQ).

Primary Outcome 2

Biomarker Normalization (NT-proBNP & hs-cTnI)

Quantitative reduction and stabilization of myocardial stress markers and lipid particle burden under physician co-signed metabolic and cardiovascular supportive protocols.

Primary Outcome 3

QTc & Arrhythmic Safety Governance

Continuous algorithm-assisted auditing of concomitant medications for additive QTc-prolongation risk and cytochrome P450 competitive clearance bottlenecks.

NeurologyEpileptologyNeuroimmunologyPediatric NeurologyAutoimmunityRheumatologyGastroenterologyCardiometabolismAutonomic HemodynamicsCellular BioenergeticsHepatologyClinical GeneticsRare DiseaseSupportive OncologyPharmacogenomicsGynecologyImmuno-EndocrinologyNeuro-Metabolic PsychiatryEPI-RESOLVENEURO-RESOLVEIMMUNO-RESOLVECARDIO-RESOLVEMETABO-RESOLVERARE-RESOLVEONCO-SHIELDENDO-RESOLVEMIND-RESOLVEConsilium
A quiet suburban street at dawn: a row of houses in soft light; in one ground-floor window a person sits at a laptop. No courier, no vehicle. The trial happens in participants' homes.