Last reviewed · How we verify

NCT05761457

Efficacy and Safety of Autologous Cryopreserved Platelets in Patients With PTR

Status unknown NA Last updated 9 March 2023
What this trial tests

NA trial testing Cryopreserved autologous platelet transfusion in Platelet Transfusion Refractoriness in 25 participants. Status unknown.

Timeline
1 March 2023
Primary endpoint
10 January 2025
10 January 2025

Quick facts

Lead sponsorThe First Affiliated Hospital of Soochow University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment25
Start date1 March 2023
Primary completion10 January 2025
Estimated completion10 January 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

The First Affiliated Hospital of Soochow University

Who can join

Adults 15 to 70, any sex, with Platelet Transfusion Refractoriness. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to improve the platelet level of PTR patients; Prevent and improve bleeding; Help patients to successfully through the bone marrow suppression period after chemotherapy; Reduce the overall rate of PTR and allo-immunity; Saving platelet resources and reducing blood burden.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Platelet Transfusion Refractoriness

Currently open trials in the same condition.

Other The First Affiliated Hospital of Soochow University 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/NCT05761457.

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