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Clinical Trials in Switzerland / NCT04732273
Recruiting Observational

The Swiss Childhood Cancer Survivor Study - Follow-up (SCCSS-FollowUp)

NCT04732273 · tracked via the Priya Life Science Switzerland tracker
Phase
Observational
Started
2022-06-20
Last updated
2025-09-23

Condition(s) studied

Late EffectChildhood Cancer

Investigational drug(s) / intervention(s)

Physical examination, diagnostic tests, laboratory testsPersonal history, questionnaire

Physical examination, diagnostic tests, laboratory tests: Physical examination, diagnostic tests depending on examined organ system (e.g. lung function test, echocardiography, audiometry), and laboratory tests (e.g. kidney parameter, hormonal levels).

Personal history, questionnaire: Personal history and focused questionnaires per organ system including symptoms, medication use, physical activity, and general wellbeing.

Study summary

The SCCSS-FollowUp is a national, multicenter cohort study designed to investigate late effects in childhood cancer survivors in a prospective and longitudinal way. The study is embedded in regular follow-up care and inclusion in the study takes place in a step-wise approach. The investigators collect data from clinical examinations, laboratory and functional tests, and questionnaires to learn more about late effects of childhood cancer treatments.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
This prospective cohort study is based on the Childhood Cancer Registry (ChCR), a national, population-based cancer registry that includes all children and adolescents in Switzerland who were diagnosed with cancer at age 0-20 years. It includes patients diagnosed with leukemia, lymphoma, central nervous system tumors, and malignant solid tumors or Langerhans cell histiocytosis. Inclusion Criteria: * Registered in the Childhood Cancer Registry (ChCR) or treated and followed-up in a Swiss pediatric oncology (SPOG) clinic, but not registered in the ChCR because of residency in neighboring countries * Diagnosed at age 0 - 20 years * Childhood cancer treatment completed * All age categories at time of inclusion in the study (children, adolescents, adults) * Written informed consent Exclusion criteria: * Childhood cancer survivors in a palliative or relapsed situation where no follow-up examinations are foreseen.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
University Childen's Hospital Basel Basel Switzerland Recruiting
University Children's Hospital Bern Bern Switzerland Recruiting
University Hospital Geneva Geneva Switzerland Recruiting

More University of Bern trials in Switzerland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04732273 on ClinicalTrials.gov ↗ ← All trials in Switzerland