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Controlled Reduction of AO Spine B3 Fractures in Ankylosing Spinal Disorders Using an Inflatable Positioning Device: Technical Note and Retrospective Single-centre Case Series

ConditionsSpine FractureOsteoporosisSpondylitis, Ankylosing
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorDiakonie-Klinikum Stuttgart

About this trial

Retrospective observational

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients were eligible if they were aged 18 years or older

Had a documented diagnosis of ankylosing spondylitis

Had an imaging-confirmed AO Spine B3 fracture,

Underwent posterior instrumented stabilization.

Disqualifiers

Patients managed non-operatively

Patients with spondylodiscitis, primary or metastatic neoplasia, or congenital spinal anomalies were excluded.

Patients with insufficient data for the predefined variables or without follow-up to the primary endpoint were excluded

Trial population

Patients with ankylozing spondylitis and B3 spine fractures

Trial design

Design model

Case-only

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Complications

Clavien-Dindo classification for complications

Time frame
12 months

Secondary outcomes

1

Hardware related complications

Complications like screw losening, screw fracture, etc

Time frame
12 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Diakonie-Klinikum Stuttgart

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: