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NCT03505086: BITE

Bleeding In Thrombocytopenia Explained

Recruiting now Last updated 21 December 2023
What this trial tests

trial testing Blood withdrawal in Hematologic Neoplasms in 1,000 participants. Currently enrolling.

Timeline
4 December 2018
Primary endpoint
1 October 2022
1 June 2026

Quick facts

Lead sponsorSanquin-LUMC J.J van Rood Center for Clinical Transfusion Research
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment1,000
Start date4 December 2018
Primary completion1 October 2022
Estimated completion1 June 2026
Sites1 location across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Sanquin-LUMC J.J van Rood Center for Clinical Transfusion Research

Who can join

18 and older, any sex, with Hematologic Neoplasms or Bleeding. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Multicenter case cohort study investigating clinical risk factors for clinically relevant bleeding in hemato-oncology patients, as well as bleeding related biomarkers during intensive treatment.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Risk factors for bleeding in haemato-oncology patients-a nested case-control study: The BITE study protocol (Bleeding In Thrombocytopenia Explained).
    Cornelissen LL, Caram-Deelder C, van der Bom JG, Middelburg RA, et al · · 2020 · cited 2× · PMID 32606056 · DOI 10.1136/bmjopen-2019-034710

Verify or expand the search:

Other trials of Blood withdrawal

Trials testing the same drug.

Other recruiting trials for Hematologic Neoplasms

Currently open trials in the same condition.

Other Sanquin-LUMC J.J van Rood Center for Clinical Transfusion Research 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/NCT03505086.

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