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The effect of zoledronic acid on the prevention and treatment of bone loss in lymphoma patient receiving first-line therapy,a multicentre ,randomised,placebo-controlledl trial

The effect of zoledronic acid on the prevention and treatment of bone loss in lymphoma patient receiving first-line therapy,a multicentre ,randomised,placebo-controlledl trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010771
Enrollment
Unknown
Registered
2017-03-03
Start date
2017-03-02
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

lymphoma

Interventions

experiment group:zoledronic acid,oral vitamin D and calcium
control group:oral vitamin D and calcium

Sponsors

Caner center,West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed lymphomas; 2. Aged 20 years or older; 3. Chemotherapy regimens include high dose glucocorticoid; 4. Creatinine clearance=2 upper limit of normal; 5. High dose glucocorticoid:dexamethasone >20mg/d,prednisone>60mg/d,methylprednisolone>75mg/d; 6. Signed informed consent documents.

Exclusion criteria

Exclusion criteria: 1. bone metastasis; 2. inhibition in the spinal cord cause by collapse; 3. Bisphosphonate used in 6 months; 4. primary hyperparathyroidism; 5. Osteomalasia; 6. Untreated hypocalcemia (ionized, iCa), before enrollment calcium levels must be within the normal range; 7. Untreated secondary hyperparathyroidism, as long as the patient in the treatment, parathyroid hormone (PTH) abnormalities can also be grouped; 8. Patients with vitamin D deficiency ( 10.2 mg / dL or ionized calcium> 1.32 mmol/L.

Design outcomes

Primary

MeasureTime frame
Bone Mineral Density;25-(OH)D3;CTX;bALP;

Countries

China

Contacts

Public ContactLiqun Zou

West China Hospital of Sichuan University

hxlcyxy@163.com+86 18980601027

Outcome results

None listed

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