Back to search results

LOG-I - Impact Study of LOG-AFTER Software on Long-term Monitoring of Former Patients (LOG-I - LOG-Impact Study)

Abroad (travel likely)Recruiting

Conditions

Pediatric Cancer · Cancer Survivor · Hemato-oncologic Patients

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • University Hospital of Angers, Angers, Maine Et Loire, France

    Contact: Study coordinator (Charlotte DEMOOR-GOLDSCHMIDT, Dr) · Charlotte.DemoorGoldschmidt@chu-angers.fr · (+33)2 41 35 38 63
    Contact: Study coordinator (Pascal VEILLON, project manager) · paveillon@chu-angers.fr · (+33)2 41 35 49 59
    Contact: Principal Investigator (Charlotte DEMOOR-GOLDSCHMIDT, Dr)
    Contact: Principal Investigator (Natacha ENTZ-WERLE, Pr)
    Contact: Principal Investigator (Amandine BERTRAND, Dr)
    Contact: Principal Investigator (Eric THEBAULT, Dr)
Study leads

  • Charlotte DEMOOR-GOLDSCHMIDT, Dr

    Principal Investigator

    University Hospital of Angers

View source on ClinicalTrials.gov(opens in a new tab)