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NCT04168788Completed

Pharmacogenetic Study of Antimitotic Therapies Involved in Hepatic VOD in Children With Nephroblastoma or ALL

Pharmacogenetic Study of Antimitotic Therapies Involved in Hepatic Veno-occlusive Disease in Children With Nephroblastoma or Acute Lymphoblastic Leukemia

Source: ClinicalTrials.gov · Last updated 29 Jun 2026

Brief summary (registry, in English)

Hepatic veno-occlusive diseases (VOD) during cancer treatment in children are serious toxicities that have occurred with interruptions of chemotherapy and risk of relapse. In addition, these toxicities have a negative impact on the patient's quality of life, serious long-term sequelae and are potentially fatal in children. The risk factors associated with the occurrence of these complications are, to date, unknown, at the exception to the exposition to certain treatments (6-thioguanine, busulfan, actinomycin D, radiotherapy, etc.). To understand the effects of this toxicity and those of susceptibility to the disease becomes a major issue in the treatment of these children.

Status (registry)
Completed
Study type
Interventional
Enrollment
85 (actual)
First submitted
5 Nov 2019
Start date
1 Jan 2020
Primary completion date
7 Jul 2025
Lead sponsor
University Hospital, Angers
NCT number
NCT04168788

What you commit to

  • Study type: Interventional
  • Participants enrolled: 85
  • From 1 Jan 2020 to the primary completion date, 7 Jul 2025
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Person under psychiatric care under duress

Other

  • Unavaibility of constitutional DNA
  • Person who receive more than one treatment line for nephroblastoma or ALL in childhood or adolescence
  • Pregnant, lactating or parturient women
  • Person deprived of their liberty by judicial or administrative decision
  • Person subject to legal protection
  • Person unable to express their consent

Who the study is looking for

  • Children aged \< 18 years old at the time of cancer diagnosis
  • Having been treated with a single line of treatment for nephroblastoma or ALL, in France between 2000 and 2018, and who did not receive allogeneic hematopoietic stem cell transplantation
  • Weight greater than 5 kg at inclusion
  • Informed consent dated and signed by the holder of the parental authority (if minor) or by the patient (if major) to take part in the study
  • Affiliated to a Social Security scheme

Age in the registry: 6 months to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Univesity Hostipal of Amiens
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AmiensFranceUnknown status
University Hospital of Bordeaux
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BordeauxFranceUnknown status
University of Brest
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BrestFranceUnknown status
Centre Oscar Lambret
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LilleFranceUnknown status
Hôpital la Timone
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MarseilleFranceUnknown status
University Hospital of NICE
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NiceFranceUnknown status
Hôpital Trousseau
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ParisFranceUnknown status
University Hospital of Poitiers
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PoitiersFranceUnknown status
University Hospital of Rennes
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RennesFranceUnknown status
University Hospital of La Réunion
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Saint-DenisFranceUnknown status
University Hospital of Tours
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ToursFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.