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Prevention of bone loss following spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN46977778
Enrollment
14
Registered
2004-09-30
Start date
2003-08-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Musculoskeletal Diseases: Osteoporosis Musculoskeletal Diseases Osteoporosis without pathological fracture

Interventions

Patients will be randomly assigned to either 1. Control group, 2. Group receiving zoledronate 3. Group receiving mechanical stimulation (vibration) and receive the treatment over a 6 month period.

Sponsors

Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients admitted to Royal National Orthopaedic Hospital (RNOH) with a spinal cord injury Added 16/04/10: 2. Female patients had to be postmenopausal, surgically sterile or willing to practice a medically acceptable form of birth control during the study period and for at least 12 months after study completion 3. All subjects gave written consent to take part in the study

Exclusion criteria

Exclusion criteria: Added 16/04/10: 1. Pregnant or breastfeeding 2. Previous history of allergic reaction to bisphosphonates 3. Previous history of iritis or uveitis 4. Significant renal impairment or evidence of vitamin D deficiency (serum 25-hydroxyvitamin D <25 nmol/L)

Design outcomes

Primary

MeasureTime frame
1. Changes in Bone Mineral Density and biochemical markers of bone metabolism over time. 2. Difference between groups

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026