Clinical Trials Logo

Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03647410
Study type Observational
Source Hebei Medical University Third Hospital
Contact Ruipeng Zhang
Phone +8615613390624
Email zhangruipengdoctor@126.com
Status Recruiting
Phase
Start date June 2011
Completion date September 2018

See also
  Status Clinical Trial Phase
Completed NCT03096470 - Closed Reduction With Anesthesia and no Anesthesia for Developmental Dislocation of the Hip < 6 Months N/A