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NCT03545659

Childhood Acute Lymphoblastic Leukaemia: Follow-Up

Completed Last updated 1 September 2021
What this trial tests

trial testing Mode of relapse/SMN detection in Precursor Cell Lymphoblastic Leukemia-Lymphoma in 277 participants. Completed in 20 January 2021.

Timeline
4 September 2018
Primary endpoint
30 December 2020
20 January 2021

Quick facts

Lead sponsorUniversity of Aarhus
StatusCompleted
Study typeOBSERVATIONAL
Enrollment277
Start date4 September 2018
Primary completion30 December 2020
Estimated completion20 January 2021
Sites5 locations across Denmark, Finland, Sweden, Norway, Iceland

Drugs / interventions tested

Conditions studied

Sponsor

University of Aarhus

Who can join

Adults 1 to 18, any sex, with Precursor Cell Lymphoblastic Leukemia-Lymphoma or Recurrence. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Over the past decades, advances in treatment have led to an increasing number of children who survive cancer, resulting in a growing population of childhood cancer survivors. After end of cancer treatment on common protocols survivors are enrolled in non-harmonized follow-up programs with frequent visits and blood samples. However, the evidence for the value of these follow-up programs with respect to the effect on detecting relapse and the effects on overall survival is scarce. The aim of the study is to give a comprehensive description of the detection mode of relapsed acute lymphoblastic leukaemia (ALL), including symptoms and blood test results. Further, we aim to evaluate if the mode of detection affects survival.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Precursor Cell Lymphoblastic Leukemia-Lymphoma

Currently open trials in the same condition.

Other University of Aarhus trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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