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TORCH-LATAM: A Regional Pathway to Improve Transplant Evaluation for Congenital Heart Disease

Study acronym: TORCH-LATAM
StatusNot Yet Recruiting
PhaseNot applicable
Started2027-03
View on ClinicalTrials.gov ↗
Congenital heart disease can progress to advanced cardiac or cardiopulmonary failure requiring heart, heart-lung, or, in selected congenital conditions, bilateral lung transplantation with cardiac repair. Access to transplant evaluation and organ utilization can vary across regions and institutions, and potential candidates who are never referred or evaluated are not represented in conventional waiting-list statistics. TORCH-LATAM is a pragmatic multicenter stepped-wedge cluster-randomized effectiveness-implementation trial evaluating the TORCH Integrated Transplant Access Pathway (TORCH-ITAP) in Latin America. Regional network clusters transition in a randomized sequence from usual care to TORCH-ITAP. The pathway standardizes early identification and referral, a common recipient dataset, multidisciplinary candidacy adjudication, structured donor-organ assessment, immunologic and anatomic-physiologic matching, preservation and transport traceability, and navigation of clinical, regulatory, logistical, and financial barriers. The primary outcome is the proportion of enrolled recipient participants who complete a standardized multidisciplinary transplant evaluation and receive a documented candidacy decision within 90 days. Secondary outcomes include activation of an official transplant pathway or waitlist where applicable, transplantation within 12 months, pretransplant death or irreversible deterioration, donor-organ utilization, post-transplant safety and survival, and implementation outcomes. Recipient participants constitute the ClinicalTrials.gov enrollment; donors, organs, donor-recipient matches, preservation strategies, and transplant episodes are nested analytic units. TORCH-ITAP does not allocate organs and does not supersede national transplant laws, authorized transplant programs, or governmental requirements for cross-border organ movement.
Trial Details
NCT Number NCT07799272
Lead Sponsor CardioVision International Tech, S.A.S. de C.V.
Collaborators: Advanced Sciences Technologies, S.A. de C.V., Advanced Science Technologies S.A.S.
Conditions Congenital Heart Disease
Enrollment 600 participants
Start Date 2027-03
Primary Completion 2029-09 (estimated)
Study Completion 2031-06 (estimated)
Updated on ClinicalTrials.gov 2026-09-02