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The Use of Bisphosphonates in the Treatment of Avascular Necrosis of the Femoral Head

T

The Hospital for Sick Children

Status

Terminated

Conditions

Femoral Head Avascular Necrosis

Treatments

Drug: Pamidronate Disodium

Study type

Interventional

Funder types

Other

Identifiers

NCT02007915
1000009396

Details and patient eligibility

About

To determine the safety and effectiveness of pamidronate in patients with radiographically proven avascular necrosis which are the result of unstable (acute) slipped capital femoral epiphysis, traumatic proximal femur fractures, traumatic hip dislocations, or idiopathic in nature.

Full description

Avascular necrosis of the femoral head and collapse is a devastating condition in the pediatric patient population leading to degenerative arthritis and significant disability. Bisphosphonate therapy has been shown to be effective in the treatment of adults with avascular necrosis of the femoral head. For children and adolescents however, there is currently no effective treatment that prevents collapse of the femoral head. Some patients with proven avascular necrosis of the femoral epiphysis are treated with bisphosphonates (intravenous pamidronate) at the The Hospital for Sick Children. The main aim of this study is to prospectively collect data on HSC patients receiving bisphosphonate treatment and thereby report the effectiveness of this treatment in the prevention of femoral head collapse.

Enrollment

20 patients

Sex

All

Ages

10 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients between the ages of 10 and 18 with:

  • unstable slipped capital femoral epiphysis (defined as inability to bear weight) or acute slipped capital femoral epiphysis (defined as a separation of the epiphysis from the metaphysis of the proximal femur) who have been pinned either in situ or following reduction,
  • traumatic hip dislocations or traumatic proximal femur fractures, or
  • "idiopathic" avascular necrosis of the femoral head which includes unknown causes as well as Sickle Cell Disease, post radiation use, post chemotherapy treatment, and post steroid treatment.

Exclusion criteria

  • Decline to participate in study. (Patients will be still offered this therapy whether or not they wish to be included in the official study protocol. Clinical evaluations, laboratory and imaging tests would be unchanged if they choose to be treated with intravenous pamidronate)
  • Significant femoral head collapse - judged radiographically by treating surgeon
  • Idiopathic causes under the age of 10.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Pamidronate Disodium
Experimental group
Treatment:
Drug: Pamidronate Disodium

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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