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Fosamax for Childhood Cancer Survivors

Primary Purpose

Osteoporosis

Status
Unknown status
Phase
Phase 3
Locations
Hong Kong
Study Type
Interventional
Intervention
Alendronate
Placebo
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoporosis focused on measuring Childhood cancer survivors, Osteoporosis, Bone mineral density, Therapy, Bisphosphonate, Randomized controlled trial

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Chinese patients who completed treatments for childhood cancers for at least 5 years
  • Currently followed up in the Department of Paediatrics of Prince of Wales Hospital
  • Younger than 18 years old at the time of diagnosis of underlying cancers
  • Evidence of osteoporosis (i.e. BMD T- or Z-score < -2.5 at lumbar spine)
  • Older than 15 years of age at the time of recruitment

Exclusion Criteria:

  • Current treatment (i.e. within 6 months) with maintenance systemic or high-dose inhaled corticosteroids
  • Subjects who cannot cooperate for BMD measurements
  • Pregnant female patients
  • Subjects with prior history of allergy to alendronate or in whom alendronate treatment is contraindicated

Sites / Locations

  • Prince of Wales Hospital, Shatin, N.T.Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Alendronate

Placebo

Arm Description

Oral alendronate 70 mg weekly

Conventional drug treatment

Outcomes

Primary Outcome Measures

The percent change in bone mineral density (BMD) at lumbar spine at 36-weeks in subjects who receive active and control treatments

Secondary Outcome Measures

Changes in BMD at femoral neck
Changes in biochemical markers of bone turnover
Occurrence of clinical bone-related symptoms at 12-weeks and end of this study

Full Information

First Posted
October 23, 2006
Last Updated
May 22, 2008
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT00391404
Brief Title
Fosamax for Childhood Cancer Survivors
Official Title
Randomized Controlled Study on the Benefits and Safety of Bisphosphonate Treatment in Childhood Cancer Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
May 2008
Overall Recruitment Status
Unknown status
Study Start Date
May 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Survivors of childhood cancers face a variety of long-term problems. The investigators' recent study found that osteoporosis and osteopenia were common among these patients. The factors leading to, as well as the best treatment option for, this morbidity are unclear. Bisphosphonates are currently the standard therapy for osteoporosis in the elderly. However, the efficacy and safety of bisphosphonates for treating osteoporosis in long-term cancer survivors have not been tested. The investigators hypothesize that alendronate, an orally active bisphosphonate, is efficacious and safe in the treatment of osteoporosis in these patients.
Detailed Description
The modern treatment for childhood malignancy includes surgery and chemoradiotherapy either individually or in combination. Despite the great achievement in improving patient survival, these treatments also greatly enhance the adverse effects on the unfortunate children. Our research group has recently conducted a pioneer study on the bone mineralization and bone mineral density (BMD) study in longterm childhood cancer survivors in local patients who have completed anti-cancer treatment for at least five years. This landmark study showed that persistent treatment-related adverse effects on skeletal development are common (up to 50%) in local long-term survivors of childhood cancers. Thus, it is important during this critical period of rapid somatic growth in adolescents and young adults that these cancer survivors achieve their peak potential for bone mineralization and strengthening. In this proposed study, we investigate with a randomized and controlled study design on the efficacy of a second-generation oral bisphosphonate, alendronate, to improve BMD over a 36-week period in long-term survivors of childhood cancers in Hong Kong. In addition to alendronate, all subjects in the active and control groups will receive alfacalcidol (vitamin D) and calcium carbonate throughout the whole study period. The study results will help paediatric oncologists to decide on the optimal remedial treatments against osteoporosis in long-term cancer survivors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
Childhood cancer survivors, Osteoporosis, Bone mineral density, Therapy, Bisphosphonate, Randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Alendronate
Arm Type
Active Comparator
Arm Description
Oral alendronate 70 mg weekly
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Conventional drug treatment
Intervention Type
Drug
Intervention Name(s)
Alendronate
Other Intervention Name(s)
Fosamax
Intervention Description
Alendronate 70 mg weekly (oral)
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
The percent change in bone mineral density (BMD) at lumbar spine at 36-weeks in subjects who receive active and control treatments
Time Frame
36 weeks
Secondary Outcome Measure Information:
Title
Changes in BMD at femoral neck
Time Frame
36 weeks
Title
Changes in biochemical markers of bone turnover
Time Frame
36 weeks
Title
Occurrence of clinical bone-related symptoms at 12-weeks and end of this study
Time Frame
36 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chinese patients who completed treatments for childhood cancers for at least 5 years Currently followed up in the Department of Paediatrics of Prince of Wales Hospital Younger than 18 years old at the time of diagnosis of underlying cancers Evidence of osteoporosis (i.e. BMD T- or Z-score < -2.5 at lumbar spine) Older than 15 years of age at the time of recruitment Exclusion Criteria: Current treatment (i.e. within 6 months) with maintenance systemic or high-dose inhaled corticosteroids Subjects who cannot cooperate for BMD measurements Pregnant female patients Subjects with prior history of allergy to alendronate or in whom alendronate treatment is contraindicated
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ting Fan Leung, MBChB, MD
Phone
852-2632 2981
Email
tfleung@cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ting Fan Leung, MBChB, MD
Organizational Affiliation
Department of Pediatrics, The Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital, Shatin, N.T.
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick MP Yuen, MD, FRCPC
First Name & Middle Initial & Last Name & Degree
Chi Kong Li, MBBS, MD
First Name & Middle Initial & Last Name & Degree
Christopher WK Lam, PhD
First Name & Middle Initial & Last Name & Degree
Vincent Lee, MBChB

12. IPD Sharing Statement

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Fosamax for Childhood Cancer Survivors

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