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AO Multicenter Intervention Trial for Prevention of Surgical Site Infection

NCT03380273 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 222

Last updated 2022-01-18

No results posted yet for this study

Summary

This study is designed to collect data from 8,476 fracture patients during a pre-and post-intervention phases of two years length each. The intervention consists on the implementation of the AOT SSI Prevention Bundle.

D

Conditions

  • Surgical Site Infection

Interventions

BEHAVIORAL

Implementation of the AO Trauma SSI Prevention Bundle

AOT SSI Prevention Bundle Preventive measure 1. Antibiotic prophylaxis 2. Perioperative antibiotics 3. Oxygen administration 4. Patient temperature 5. Surgeon protective wear 6. Patient operative skin preparation 7. Suction drains 8. Blood glucose level 9. Red cell transfusion 10. Dressing changes

Sponsors & Collaborators

  • AO Clinical Investigation and Publishing Documentation

    lead OTHER

Principal Investigators

  • Stephen Kates, MD · VCU Health

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SEQUENTIAL

Eligibility

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

Timeline & Regulatory

Start
2019-12-06
Primary Completion
2021-12-30
Completion
2021-12-31

Countries

  • United States
  • Argentina
  • Germany
  • Romania
  • South Korea
  • Spain

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 NCT03380273 on ClinicalTrials.gov