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NCT05703633: REVIVEME

Transplantation of Uncontrolled DCD Kidneys REconditioned by a Novel Ex-VIVo Perfusion MEthod

Status unknown Phase 1, PHASE2 Last updated 31 January 2023
What this trial tests

Phase 1, PHASE2 trial testing uDCD treatment in End-Stage Kidney Disease in 8 participants. Status unknown.

Timeline
21 August 2023
Primary endpoint
31 August 2024
31 December 2024

Quick facts

Lead sponsorSahlgrenska University Hospital
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment8
Start date21 August 2023
Primary completion31 August 2024
Estimated completion31 December 2024

Drugs / interventions tested

Conditions studied

Sponsor

Sahlgrenska University Hospital

Who can join

Adults 18 to 65, any sex, with End-Stage Kidney Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Eight patient will be transplanted with kidneys from donors dying after uncontrolled circulatory arrest (uDCD), with prolonged warm ischemia (up to 4,5 hours), preserved by a new method based on removal of fibrinogen/fibrin in the capillary systems, leading to an effective oxygenation of the tissue using an ex-vivo hospital manufactured perfusion device, minimizing the risk for ischemia-reperfusion injury (I/R-I) after kidney transplantation.Each patient will be studied for three months, with long-term follow-up data collected at 6 and 12 months

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for End-Stage Kidney Disease

Currently open trials in the same condition.

Other Sahlgrenska University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05703633.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing