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Lumbopelvic Fixation Versus Novel Adjustable Plate for Displaced Sacral Fracture

H

Hebei Medical University Third Hospital

Status

Unknown

Conditions

Reduction Deformity of Limb

Treatments

Device: lumbopelvic fixation

Study type

Observational

Funder types

Other

Identifiers

NCT03647410
RPZ2018

Details and patient eligibility

About

Patients of unilaterally displaced sacral fractures fixed with lumbopelvic technique or novel adjustable plate from June 2011 to June 2017 were recruited into this study and were divided into two groups: group A (lumbopelvic fixation) and groups B (novel adjustable plate). Surgical time, intraoperative blood loss, frequency of intraoperative fluoroscopy, reduction quality, related complications were reviewed. Fracture healing was assessed by the radiographs conducted at follow-up. Functional outcome was evaluated according to the Majeed score at the final follow-up.

Full description

Patients of unilateral displaced sacral fractures from June 2011 to June 2017 were recruited into this study. The inclusion criteria were as follows: 18-65 years, with normal activity ability before injury, fixed with lumbopelvic technique or novel adjustable plate, completed more than a year follow-up. The exclusion criteria were as follows: pathologic fractures, open fractures, associated with other severe injuries (traumatic brain injury), risk factors affecting bone healing (osteoporosis, smoking, and metabolic diseases) and non-completion of one-year follow-up. Surgical time, intraoperative blood loss, frequency of intraoperative fluoroscopy, related complications were reviewed. Reduction quality was assessed on the postoperative radiographs and CT scans. Functional outcome was evaluated according to the Majeed score system at the final follow-up.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-65 years, with normal activity ability before injury
  • Fixed with lumbopelvic technique or novel adjustable plate
  • Completed more than a year follow-up

Exclusion criteria

  • Pathologic fractures
  • Open fractures
  • Associated with other severe injuries (traumatic brain injury)
  • Risk factors affecting bone healing (osteoporosis, smoking, and metabolic diseases)
  • Non-completion of one-year follow-up

Trial design

20 participants in 2 patient groups

lumbopelvic fixation
Description:
sacral fractures fixed with lumbopelvic fixation
novel adjustable plate
Description:
sacral fractures fixed with novel adjustable plate
Treatment:
Device: lumbopelvic fixation

Trial contacts and locations

1

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Central trial contact

Ruipeng Zhang

Data sourced from clinicaltrials.gov

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