Clinical Trials Directory

Trials / Unknown

UnknownNCT03647410

Lumbopelvic Fixation Versus Novel Adjustable Plate for Displaced Sacral Fracture

Lumbopelvic Fixation Versus Novel Adjustable Plate for Displaced Sacral Fractures: A Retrospective Cohort Study

Status
Unknown
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
Hebei Medical University Third Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers

Summary

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DEVICElumbopelvic fixationSacral fractures fixed with lumbopelvic fixation or novel adjustable plate were divided into two groups. Surgical time, intraoperative blood loss, frequency of intraoperative fluoroscopy, reduction quality, related complications, and functional outcome were reviewed.

Timeline

Start date
2011-06-01
Primary completion
2018-09-01
Completion
2018-09-01
First posted
2018-08-27
Last updated
2018-08-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03647410. Inclusion in this directory is not an endorsement.