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Bone Strength After Spinal Cord Injury

Impact of Spinal Cord Injury on Bone Strength in Paralysed Extremities.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01853488
Enrollment
273
Registered
2013-05-15
Start date
2010-10-31
Completion date
2015-11-30
Last updated
2024-02-13

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

Conditions

Spinal Cord Injury

Keywords

Osteoporosis, BMD, SCI, DXA, pQCT

Brief summary

Background: After a traumatic spinal cord injury, a severe bone loss in the paralyzed extremities is observed. This leads to a osteoporosis which is connected to a high fracture risk. Aims: To compare the two measurement methods DEXA and pQCT concerning optimal diagnostics and assessment of fracture risk in subjects with spinal cord injury. Subjects: 250 women and 250 men (age≥18, any AIS-classification) with an acute or chronic spinal cord injury will be recruited for this study. For a reference group, 500 able-bodied persons will be measured analogously. Methods: Using DEXA-Osteodensitometry, bone parameters of the lumbar vertebral column, proximal femur, distal radius, distal tibia and knee area will be assessed. Additionally, geometric bone parameters of the tibia will be measured by using pQCT. All measurements will be done unilaterally. For the assessment of potential risk factors for reduced bone stiffness after spinal cord injury a questionnaire will be used.

Interventions

RADIATIONDXA

Osteodensitometry

RADIATIONpQCT

Osteodensitometry

Sponsors

Swiss Paraplegic Research, Nottwil
Lead SponsorNETWORK

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Spinal Cord Injury * mobilized patients * written informed consent

Exclusion criteria

* current fracture * limited mobility * contractures of the lower limbs * decubitus ulcer * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Bone parametersjust one timepointMeasurement of the extremities with DEXA and pQCT

Secondary

MeasureTime frameDescription
Fracturesjust one timepoint (questionnaire)Number of fractures since SCI

Countries

Switzerland

Outcome results

None listed

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