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The prospective clinical study of zoledronic acid in the prevention of steroid-related bone disease after chemotherapy in acute lymphoblastic leukemia

The prospective clinical study of zoledronic acid in the prevention of steroid-related bone disease after chemotherapy in acute lymphoblastic leukemia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031553
Enrollment
Unknown
Registered
2020-04-04
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-04-06

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

Conditions

Acute lymphoblastic leukemia

Interventions

preventive intervention:Zoledronic acid combined with calcium , vitamin D
therapeutic intervention:Zoledronic acid combined with calcium , vitamin D

Sponsors

Shanghai Institute of Hematology, Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male or female patients aged 18-65 years; 2. Patients with primary acute lymphoblastic leukemia; 3. Patients without serious heart disease or coronary heart disease history; 4. Patients with liver and kidney function suitable for chemotherapy: SGOT and SGPT should not exceed 2 times of the upper limit of normal; total bilirubin in serum should not exceed 1.5 times of the upper limit of normal; 5. Patients with normal amylase and no previous history of pancreatitis; 6. Patients willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrollable diabetes; 2. HIV and syphilis infected patients; 3. Pregnant or lactating women; 4. Patients who have received organ transplantation in the past; 5. Patients with serious neurological or psychiatric history.

Design outcomes

Primary

MeasureTime frame
Bone metabolism (bone density, serum bone metabolism indicators);

Secondary

MeasureTime frame
CR;overall survival, OS;minimal residual disease, MRD;safety;

Countries

China

Contacts

Public ContactJin Wang

Shanghai Institute of Hematology, Ruijin Hospital Affiliated to Shanghai Jiaotong University School of medicine

jinwang@shsmu.edu.cn+86 13524945202

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026