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Osteonecrosis in Children With Acute Lymphoblastic Leukemia

Steroid Induced Osteoporosis in the Pediatric Population Ancillary Study- Osteonecrosis in Children With Acute Lymphoblastic Leukemia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01104324
Enrollment
130
Registered
2010-04-15
Start date
2009-07-31
Completion date
2012-12-31
Last updated
2010-04-15

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

Conditions

Acute Lymphoblastic Leukemia, Osteonecrosis

Keywords

bone health, Osteonecrosis, acute lymphoblastic leukemia

Brief summary

Acute lymphoblastic leukemia is the most common form of childhood cancer with current treatment survival rates approaching 80%. Improved outcomes show an increased number of survivors at risk for long-term treatment related side effects including osteonecrosis. Osteonecrosis, or bone death, is caused by blood supply loss to the bone causing pain and poor quality of life. The hips, shoulders, knees and ankles may be affected. Pain is the usual presenting symptom and may become severe requiring surgical decompression or replacement of the affected joint. Long-term effects including arthritis and progressive joint difficulties will not be known for decades. This study aims to determine the risk factors for developing osteonecrosis that will lead to information for earlier detection and prevention. The study will be the basis for future intervention and prevention trials.

Interventions

None listed

Sponsors

C17 Council
CollaboratorOTHER
Halton, Jacqueline, M.D.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Enrollment in the STOPP-CIS study * Informed consent of patient or care givers * \>5 years of age at MRI assessment

Exclusion criteria

* Individuals with a history of claustrophobia precluding MRI assessment

Design outcomes

Primary

MeasureTime frameDescription
osteonecrosis 1 year post leukemia therapyOne year after completion of therapy for leukemiaEach participant will undergo MRI of hip, knee, ankle and shoulder to look for ON

Secondary

MeasureTime frameDescription
Is Bone loss/failure to accure bone mineral and ONOne year post leukemia therapyIs bone loss/failure to accrue bone mineral at a normal rate during chemotherapy is/are associated with the development of ON.These patients are a subset of a lagre study where Bone mass is being measured by DEXA. We will be able to access this data to look for bone loss
Glucocorticoid dose and ONOne year post Leukemia therapyIs there a glucocorticoid threshold dose, above which patients are more likely to develop ON. These patients are a subset of a lagre study where glucocorticoid dose is recorded. We will be able to access this data.
Methotrexate dose and ONOne year post leukemia therpyIs there a methotrexate threshold dose, above which patients are more likely to develop ON. These patients are a subset of a lagre study where Methotrexate dose is recorded. We will be able to access this data.
Bone mass density and OsteonecrosisOne year post therapy for leukemiaIs reductions in bone mass density at diagnosis of leukemia associated with the development of ON. These patients are a subset of a lagre study where Bone mass is being measured by DEXA. We will be able to access this data to look for bone mass density
Weight bearing and non weight bearing activities and ONOne year post leukrmia therapyDoes weight bearing and non-weight bearing activities play a role in the development of ON. These patients are a subset of a larger study. They are recording these activities. We will be able to use this data.
Hyperlipidemia and OnOne year post leukemia therapyIs hyperlipidemia associated with the development of ON. Statins (cholesterol lowering medications) have been suggested as a therapeutic intervention to prevent ON. Fasting blood will be tested for lipids at at least one year post chemtherapy.
Thrombophilia and ONOne year post leukemia therapyIs thrombophilia associated with the development of ON. Blood will be tested at study entry following one year completion of chemotherapy.Blood will be drawn for protein C, protein S, antithrombin, activated protein C resistance, Factor V Leiden, prothrombin gene complex, MTHFR, lupus anticoagulant and antiphospholipid antibodies and Lipoprotein A.
Obesity and ONOne year post leukemia therapyIs obesity either at diagnosis or during therapy associated with ON. These patients are a subset of a larger group in a larger study. They are recording height weight and BMI. We will be able to access this data.

Countries

Canada

Contacts

Primary ContactJacqueline Halton
613 737 7600
Backup ContactLynda Hoey
613 737 7600

Outcome results

None listed

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