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Impact of Associated Abdominal Injuries on Clinical and Operative Outcome in Pelvic Injuries

Impact of Associated Abdominal Injuries on Clinical and Operative Outcome in Pelvic Fractures - a Multicenter Study From the German Pelvic Registry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03952026
Enrollment
16359
Registered
2019-05-16
Start date
2018-12-06
Completion date
2019-05-10
Last updated
2019-05-16

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

Conditions

Abdominal Trauma, Acetabular Fracture, Pelvic Ring Fracture, Polytrauma

Keywords

Pelvic trauma, Pelvic ring fracture, Acetabular Fracture, Abdominal Trauma, Polytrauma, Reduction quality

Brief summary

Pelvic fractures are severe injuries which require advanced orthopedic surgical skills to treat. On the other hand, abdominal injuries are severe injuries, which might require quick general surgical treatment. The combination of both injuries is a challenge for orthopedic surgeons, as the abdominal injury might lead to a delayed surgical treatment of the pelvic fracture. Whether an associated abdominal injury influences the quality of care of pelvic fractures, is aim of this registry study.

Detailed description

The German Pelvic Registry of the German Trauma Society is a multicenter prospective registry which collects data of patients with pelvic injuries since 2003. Beside demographic data (including concomitant injuries) allowing for epidemiological evaluations of the development of surgical care in these patients, namely the operative care is focus of this registry. Beside the chosen procedure or surgical approach, this includes both intraoperative data like time until operation, duration of the procedure or intraoperative blood loss and reduction parameters (pre- and postoperative fracture steps). The clinical course is recorded also including overall morbidity, overall mortality and osteosynthesis-related complications. The influence of a concomitant abdominal trauma on the quality of care regarding operative parameters like reduction quality or the clinical course in pelvic injuries has not been investigated yet. The investigators therefore retrospectively analyze the prospective consecutive data of patients from the multicenter German Pelvic Registry of the German Trauma Society in the years 2003 - 2017. Demographic, clinical and operative parameter were recorded and compared in two groups (isolated pelvic fracture vs. combined abdominal/pelvic trauma).

Interventions

PROCEDUREosteosynthesis of the pelvis

Osteosynthetic Fixation of the pelvic fracture

Sponsors

BG Trauma Center Tuebingen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Pelvic fracture

Exclusion criteria

* no agreement to participate in the registry

Design outcomes

Primary

MeasureTime frameDescription
Matta Gradingthrough study completion, at least 1 year after inclusionQuality of the reduction of the pelvic fracture measured in mm residual step at the fracture's site. A residual step of 0-2mm is graded as an anatomical reduction (=Matta 1), a residual step of 2-3mm is graded as an Imperfect reduction (=Matta 2) and a residual step \>3mm is graded as a poor reduction (=Matta 3).
Overall morbiditythrough study completion, at least 1 year after inclusionRate of overall complications

Secondary

MeasureTime frameDescription
osteosynthesis-associated complicationsthrough study completion, at least 1 year after inclusionRate of osteosynthesis-associated complications
length of hospital staythrough study completion, at least 1 year after inclusionDuration of the inpatient Treatment, measured in days.
Time until definitive pelvic surgerythrough study completion, at least 1 year after inclusionThe time until the definitive surgical procedure for the pelvic fracture, measured in days.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026