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Intravenous Zoledronic Acid for the Treatment of Osteoporosis and Osteonecrosis in Children With Leukemia: A Pilot Study

Intravenous Zoledronic Acid for the Treatment of Osteoporosis and Osteonecrosis in Children With Leukemia: A Pilot Study

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02632903
Enrollment
0
Registered
2015-12-17
Start date
2016-10-31
Completion date
2018-08-20
Last updated
2018-08-22

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

Conditions

Acute Lymphoblastic Leukemia, Osteonecrosis, Osteoporosis

Brief summary

This study explores the effect of zoledronic acid on incident vertebral fractures and osteonecrotic lesions in children recently diagnosed with acute lymphoblastic leukemia.

Interventions

DRUGZoledronic acid

Sponsors

Children's Hospital of Eastern Ontario
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

1. Subject or subject's legally acceptable representative has provided informed consent. 2. Children aged 8 to 16 years at the time of enrolment with a confirmed diagnosis of acute lymphoblastic leukemia (ALL). 3. Children with vertebral fractures or osteonecrotic lesions according to the following criteria: 1. children with vertebral fractures on lateral spine x-ray and/or osteonecrotic lesions on MRI of the hips and/or knees identified through routine clinical screening at least 8 weeks following chemotherapy initiation OR 2. children with vertebral fractures on lateral spine x-ray and/or osteonecrotic lesions of the hips and/or knees on MRI that are identified at any time in the first 12 months after chemotherapy initiation following presentation with back pain (in the case of vertebral fractures, identified by lateral spine x-rays) and/or hip pain (in the case of osteonecrotic lesions, identified by MRI) and/or knee pain (in the case of osteonecrotic lesions, identified by MRI).

Exclusion criteria

1. Any child for whom the treating physician feels participation is not advised. 2. Prior treatment with an osteoporosis agent (e.g. bisphosphonate). 3. Co-morbidities affecting musculoskeletal health (e.g. cerebral palsy). 4. Children with renal failure (eGFR\<60ml/min/1.73m2). 5. Children with untreated vitamin D deficiency (vitamin D \<50nmol/L). 6. Children with hypocalcemia. 7. Children planning dental procedures and/or dental surgery during the course of the study. 8. Children with asthma who are acetylsalicylic acid (ASA) sensitive. 9. Children with a documented history of atrial fibrillation. 10. Currently pregnant or planning a pregnancy during the study. 11. Currently breastfeeding or planning on breastfeeding during the study.

Design outcomes

Primary

MeasureTime frameDescription
To assess the effect of zoledronic acid on preventing incident vertebral fractures15 months post-diagnosis (12 months after baseline visit)To assess the effect of zoledronic acid on preventing incident vertebral fractures as measured by lateral spine radiographs at 15 months post-diagnosis compared to baseline (with baseline occurring 3 months post-diagnosis). An incident vertebral fracture on lateral spine radiographs will be defined as a new fracture (Genant Grade 1 or more) in a previously normal vertebral body, or worsening of an existing fracture (increase in Genant Grade by at least 1) on the follow-up x-ray that takes place 12 months after the first dose.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026