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Clinical Priority Program-Bone Infection Registry

NCT01677000 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 297

Last updated 2020-08-13

No results posted yet for this study

Summary

Establish an international registry of over 400 patients with deep infections involving the bone and/or joint from≥20 centers representing all regions of the world with varied hospital and surgeon practice settings to ensure that registry analyses and research reflect typical clinical practice thereby providing optimal guidance for patients, clinicians, and healthcare researchers. Using a data collection platform that minimizes entry burden, collects most information at the time of surgery, and uses Internet technology to minimize data entry. The registry will include:

1. baseline patient attributes;
2. surgical approach, implants and technology;
3. hospital course;
4. surgeon and institutional characteristics;
5. longitudinal patient outcome,
6. post-procedure complications and revisions,
7. serum/tissue/drainage samples.

Conditions

  • Bone Infection
  • Staphylococcus Aureus

Sponsors & Collaborators

  • AO Clinical Investigation and Publishing Documentation

    lead OTHER

Principal Investigators

  • Stephen L Kates, MD · University of Richmond

Eligibility

Min Age
18 Years
Max Age
130 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2018-12-31
Completion
2019-06-30

Countries

  • United States
  • Argentina
  • Austria
  • Belgium
  • Canada
  • China
  • Denmark
  • Germany
  • Japan
  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01677000 on ClinicalTrials.gov