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Construction of a Structured Follow-up Model and Multicenter Prospective Study of Late-Effect Burden in Long-term Survivors of Childhood Hematological Malignancies (HEM-SURVIVE)

Construction of a Structured Follow-up Model and Multicenter Prospective Study of Late-Effect Burden in Long-term Survivors of Childhood Hematological Malignancies (HEM-SURVIVE)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121149
Enrollment
Unknown
Registered
2026-03-26
Start date
2026-03-31
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric tumor

Interventions

HEM-SURVIVE structured follow-up model group:None
Conventional follow-up model group:None

Sponsors

Children's Hospital,Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 21 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with pediatric malignant hematologic tumors (acute lymphoblastic leukemia ALL, acute myeloid leukemia AML, lymphoma, etc.); 2. Completed primary tumor treatment (end of maintenance therapy or post-transplant) >= 12 months; 3. Currently no active tumor, in complete remission (CR) or stable condition; 4. Age 1–21 years (under 18 at initial diagnosis); 5. Able to complete follow-up and data collection, with informed consent signed by patient or guardian.

Exclusion criteria

Exclusion criteria: 1. Currently undergoing active treatment for tumor recurrence, progression, or secondary malignant tumors; 2. Complicated by severe organ dysfunction, severe psychiatric disorders, cognitive impairment, or neurological diseases, making follow-up evaluation impossible; 3. Complicated by other major genetic or systemic diseases that may significantly affect growth and development/organ function; 4. Severe non-tumor diseases with an expected survival of less than 1 year; 5. Poor expected follow-up compliance or refusal to participate.

Design outcomes

Primary

MeasureTime frame
Incidence of a composite endpoint of severe late effects (Grade 3 or higher);

Secondary

MeasureTime frame
Compliance rate of the structured follow-up model;Change in Quality of Life (QoL) scale scores;

Countries

China

Contacts

Public ContactZhang Jingying

Children's Hospital,Zhejiang University School of Medicine

Zhangjy423@126.com+86 571 8103 5912

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026