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Zoledronic Acid Administration in Acute Spinal Cord Injury

Primary Purpose

Disuse Osteoporosis

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Zoledronic acid
Sponsored by
James J. Peters Veterans Affairs Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Disuse Osteoporosis focused on measuring Spinal Cord Injury, Disuse Osteoporosis, Zoledronic acid, Bisphosphonates, Dual Energy X-ray Absorptiometry

Eligibility Criteria

18 Years - 49 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Within 3 months of the date of acute SCI.
  2. Motor-complete and incomplete SCI [American Spinal Injury Association Impairment Scale (AIS) of sensorimotor impairment (AIS A, B, and C)]

Exclusion Criteria:

  1. Extensive life-threatening injuries (in addition to SCI)
  2. Femur or tibia fracture or extensive bone trauma
  3. History of prior bone disease (Paget's disease, overactive parathyroid, osteoporosis)
  4. Post-menopausal women
  5. Known allergy to bisphosphonates
  6. Severe underlying chronic illness
  7. Current diagnosis of cancer or history of cancer
  8. I am currently receiving corticosteroids
  9. Pregnancy or lactation
  10. I have been diagnosed with kidney problems
  11. As determined from the prescreening blood tests by the study physician Serum creatinine > 2.0 mg/dl
  12. As determined from the prescreening blood tests by the study physician Corrected calcium < 8 mg/dl or > 11 mg/dl
  13. As determined from the prescreening blood tests by the study physician Elevated liver function enzymes > 2 x upper limit of normal (ULN)
  14. I am taking a bisphosphonate for heterotopic ossification (HO) (an overgrowth of bone typically diagnosed shortly after SCI in the pelvic region)
  15. I have an existing dental condition or dental infection.

Sites / Locations

  • Kessler Institute for Rehabilitation

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Zoledronic acid

No Intervention

Arm Description

At baseline, study subjects in the treatment group will receive 5 mg of zoledronic acid (Reclast: 5 mg; Novartis Pharmaceuticals Inc., East Hanover, NJ) by intravenous infusion over 30 minutes.

Participants will receive no therapy and serve as a control group and have the same outcome measures completed at parallel time points.

Outcomes

Primary Outcome Measures

Bone Mineral Density (BMD) at the Distal Femur and Proximal Tibia at Baseline and Month 12.
An imaging method known as dual energy x-ray absorptiometry (DXA) was used to obtain BMD of the distal femur and proximal tibia by using a customized research software program supplied by the manufacturer. This measurement will be the primary determinant (dependent measure) of difference among the treatment and control groups, and they will be followed over time at the previously specified time points.

Secondary Outcome Measures

Bone Mineral Density (BMD) at the Total Hip at Baseline and Month 12
An imaging method known as dual energy x-ray absorptiometry (DXA) was used to obtain BMD of the total hip.

Full Information

First Posted
January 21, 2014
Last Updated
March 12, 2018
Sponsor
James J. Peters Veterans Affairs Medical Center
Collaborators
Kessler Institute for Rehabilitation
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1. Study Identification

Unique Protocol Identification Number
NCT02042872
Brief Title
Zoledronic Acid Administration in Acute Spinal Cord Injury
Official Title
The Efficacy of Zoledronic Acid in the Prevention of Bone Loss in Acute Spinal Cord Injury
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
James J. Peters Veterans Affairs Medical Center
Collaborators
Kessler Institute for Rehabilitation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In subjects with acute SCI: To compare the effects of parenteral zoledronic acid therapy on preservation of regional and total skeletal mass (DXA). Hypothesis: Zoledronic acid will dramatically diminish bone loss in persons with acute SCI, as evidenced by serial densitometry determinations (DXA).
Detailed Description
Immobilization is associated with disuse osteoporosis. Spinal cord injury (SCI) produces a syndrome of acute skeletal immobilization with immediate and irreversible unloading of the involved skeletal regions resulting in accelerated bone loss. In addition to rapid bone loss, there are also the complications of hypercalciuria, hypercalcemia, nephrolithiasis, and renal insufficiency. In some reports, as much as 50% of regional bone mass has been lost within the first year after paralysis. A depletion of regional bone of such magnitude greatly increases the risk of fractures, with associated morbidity and increased cost of care. Often, these fractures occur with minimal or non-obvious trauma and may pass undiagnosed for varying lengths of time due to the absence of pain sensation. The acute complications of fracture may include hemorrhage, deep venous thrombosis, and autonomic dysreflexia. Long-term complications include functional deformity, non-union, infection, heterotopic calcification, and significantly longer healing time. The sociology-economic consequences include a minimum of 1 to 2 weeks of hospitalization and the potential need for an increased level of attendant care. This study will address the efficacy of a bisphosphonate, zoledronic acid (Reclast: 5 mg; Novartis Pharmaceuticals Inc., East Hanover, NJ), in the prevention of the bone loss associated with acute SCI. Prevention of regional osteoporosis in persons with SCI would reduce the morbidity associated with fractures, a known secondary complication of immobilization. Thus, the quality of life would be improved in terms of employment responsibilities (reduction in days absent from employment and income lost) and personal activities (recreational endeavors, independence, and ease in which one performs activities of daily living). Individuals with SCI may then engage more securely in activities without fear of fracture, a tremendous psychological benefit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Disuse Osteoporosis
Keywords
Spinal Cord Injury, Disuse Osteoporosis, Zoledronic acid, Bisphosphonates, Dual Energy X-ray Absorptiometry

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zoledronic acid
Arm Type
Experimental
Arm Description
At baseline, study subjects in the treatment group will receive 5 mg of zoledronic acid (Reclast: 5 mg; Novartis Pharmaceuticals Inc., East Hanover, NJ) by intravenous infusion over 30 minutes.
Arm Title
No Intervention
Arm Type
No Intervention
Arm Description
Participants will receive no therapy and serve as a control group and have the same outcome measures completed at parallel time points.
Intervention Type
Drug
Intervention Name(s)
Zoledronic acid
Other Intervention Name(s)
Zometa, Reclast
Intervention Description
At baseline, study subjects in the treatment group will receive 5 mg of zoledronic acid (Reclast: 5 mg; Novartis Pharmaceuticals Inc., East Hanover, NJ) by intravenous infusion over 30 minutes.
Primary Outcome Measure Information:
Title
Bone Mineral Density (BMD) at the Distal Femur and Proximal Tibia at Baseline and Month 12.
Description
An imaging method known as dual energy x-ray absorptiometry (DXA) was used to obtain BMD of the distal femur and proximal tibia by using a customized research software program supplied by the manufacturer. This measurement will be the primary determinant (dependent measure) of difference among the treatment and control groups, and they will be followed over time at the previously specified time points.
Time Frame
Baseline and 12 months
Secondary Outcome Measure Information:
Title
Bone Mineral Density (BMD) at the Total Hip at Baseline and Month 12
Description
An imaging method known as dual energy x-ray absorptiometry (DXA) was used to obtain BMD of the total hip.
Time Frame
Baseline and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Within 3 months of the date of acute SCI. Motor-complete and incomplete SCI [American Spinal Injury Association Impairment Scale (AIS) of sensorimotor impairment (AIS A, B, and C)] Exclusion Criteria: Extensive life-threatening injuries (in addition to SCI) Femur or tibia fracture or extensive bone trauma History of prior bone disease (Paget's disease, overactive parathyroid, osteoporosis) Post-menopausal women Known allergy to bisphosphonates Severe underlying chronic illness Current diagnosis of cancer or history of cancer I am currently receiving corticosteroids Pregnancy or lactation I have been diagnosed with kidney problems As determined from the prescreening blood tests by the study physician Serum creatinine > 2.0 mg/dl As determined from the prescreening blood tests by the study physician Corrected calcium < 8 mg/dl or > 11 mg/dl As determined from the prescreening blood tests by the study physician Elevated liver function enzymes > 2 x upper limit of normal (ULN) I am taking a bisphosphonate for heterotopic ossification (HO) (an overgrowth of bone typically diagnosed shortly after SCI in the pelvic region) I have an existing dental condition or dental infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William A Bauman, M.D.
Organizational Affiliation
James J. Peters VA Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kessler Institute for Rehabilitation
City
West Orange
State/Province
New Jersey
ZIP/Postal Code
07052
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17417700
Citation
Shapiro J, Smith B, Beck T, Ballard P, Dapthary M, BrintzenhofeSzoc K, Caminis J. Treatment with zoledronic acid ameliorates negative geometric changes in the proximal femur following acute spinal cord injury. Calcif Tissue Int. 2007 May;80(5):316-22. doi: 10.1007/s00223-007-9012-6. Epub 2007 Apr 7.
Results Reference
background
PubMed Identifier
20358358
Citation
Bubbear JS, Gall A, Middleton FR, Ferguson-Pell M, Swaminathan R, Keen RW. Early treatment with zoledronic acid prevents bone loss at the hip following acute spinal cord injury. Osteoporos Int. 2011 Jan;22(1):271-9. doi: 10.1007/s00198-010-1221-6. Epub 2010 Apr 1.
Results Reference
background

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Zoledronic Acid Administration in Acute Spinal Cord Injury

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