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NCT05188339

The Effectiveness and Safety of 4% Sodium Citrate as a Lock Solution in Central Venous Hemodialysis Catheter

Status unknown Phase 2, PHASE3 Last updated 25 July 2022
What this trial tests

Phase 2, PHASE3 trial testing 4% sodium citrate in Central Venous Catheter Thrombosis in 120 participants. Status unknown.

Timeline
20 July 2022
Primary endpoint
31 December 2022
31 December 2022

Quick facts

Lead sponsorChang Gung Memorial Hospital
PhasePhase 2, PHASE3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment120
Start date20 July 2022
Primary completion31 December 2022
Estimated completion31 December 2022
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Chang Gung Memorial Hospital

Who can join

20 and older, any sex, with Central Venous Catheter Thrombosis or Renal Dialysis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Studies that used a dilute citrate formulation (4%) demonstrated efficacy as an anticoagulant with minimal to no risk of bleeding in HD sessions. This study will compare effectiveness and safety utilizing 4% sodium citrate vs. heparin as a lock solution in central venous hemodialysis catheter among hemodialysis patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Chang Gung Memorial Hospital trials

Trials by the same sponsor.

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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/NCT05188339.

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