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Compare the outcome of dexamethasone and prednisone during remission induction for intermediate/high-risk Acute Lymphoblastic Leukemia patients:A multi-institutional randomized study

Compare the outcome of dexamethasone and prednisone during remission induction for intermediate/high-risk Acute Lymphoblastic Leukemia patients:A multi-institutional randomized study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036056
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Acute Lymphoblastic Leukemia

Interventions

prednisone : prednisone

Sponsors

Shanghai Jiaotong university school of medicine affiliated Shanghai children's medical center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 1 month to 18 years; 2. Diagnosis of acute lymphoblastic leukemia by bone marrow morphology; 3. Diagnosis of ALL by immunophenotyping.

Exclusion criteria

Exclusion criteria: 1. sIgM+; 2. Acute leukemias of ambiguous lineage diagnosed according to WHO or EGIL criteria; 3. ALL evolved from chronic myeloid leukemia (CML); 4. Down's syndrome, or major congenital or hereditary disease with organ dysfunction; 5. Secondary leukemia; 6. Known underlying congenital immunodeficiency or metabolic disease; 7. Congenital heart disease with cardiac insufficiency; 8. Treated with glucocorticoids for >=14 days, or ABL kinase inhibitors for > 7 days within one month before enrollment, or any chemotherapy or radiotherapy within 3 months before enrollment (except for emergency radiotherapy to relieve airway compression); 9. Low risk patients.

Design outcomes

Primary

MeasureTime frame
EFS;

Secondary

MeasureTime frame
OS;relapse CIN;

Countries

China

Contacts

Public ContactShuhong Shen

Shanghai Children's Medical Center

shenshuhong@scmc.com.cn+86 21-38626161-82055

Outcome results

None listed

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