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Sagittal Spinopelvic Parameters in Patients With Lower Extremity Amputation

Sagittal Spinopelvic Parameters in Patients With Lower Extremity Amputation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05318508
Enrollment
30
Registered
2022-04-08
Start date
2022-04-10
Completion date
2023-06-20
Last updated
2024-05-14

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

Conditions

Amputation, Traumatic, Low Back Pain

Brief summary

The aim of this study is to investigate the relationship between sagittal spinopelvic parameters and low back pain and quality of life in individuals with lower extremity amputation.

Detailed description

Low back pain is one of the secondary health problems that negatively affect functionality, independence and quality of life in individuals with lower extremity amputation. The prevalence of low back pain was reported to be higher in individuals with lower extremity amputation (52-89%) than in the non-amputee population (12-45%). Although the etiology of low back pain is multifactorial, changing anatomy and biomechanics after lower extremity amputation and maintaining daily activities are often associated with the development of low back pain. Postural imbalance, which is one of the musculoskeletal disorders of the spine that contributes to low back pain, is considered to cause additional load on the spinal structures.

Interventions

OTHERMeasurements of sagittal spinopelvic parameters

Sagittal spinopelvic parameters will be measured from lateral cervicothoracolumbar radiographs of patients with lower extremity amputation.

Sponsors

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged ≥ 18 and ≤ 65 years * Patients followed for at least 12 months with lower extremity amputation * Patients who have been using prosthesis for at least 3 months * Patients with stable medical and psychological status * Patients willing to participate in the study

Exclusion criteria

* Patients with serious cardiovascular, pulmonary, neurological disease or other musculoskeletal problems (inflammatory rheumatic disease, active synovitis, severe low back pain, hip/knee joint replacement or other hip/knee-related trauma, fracture, or surgery) that impair walking * Patients with severe vision, hearing and language problems

Design outcomes

Primary

MeasureTime frameDescription
Thoracic kyphosisbaselineThe angle between the line drawn perpendicular to the line through the T4 upper end plate and the lines drawn perpendicular to the line through the T12 lower end plate.

Secondary

MeasureTime frame
Cervical lordosisbaseline
Lumbar lordosisbaseline
Pelvic tiltbaseline
Pelvic incidencebaseline

Countries

Turkey (Türkiye)

Outcome results

None listed

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