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Use of Antibiotic Carrier in Acute Periprosthetic Infections (APPI) of Total Knee Replacements

M

Michael Muldoon, M.D.

Status

Withdrawn

Conditions

Infection

Treatments

Procedure: APPI of TKR-Stimulan

Study type

Observational

Funder types

Other

Identifiers

NCT02107924
1112-0211

Details and patient eligibility

About

The purpose of the study is to gather information on the use of Stimulan, the surgery, and anitbiotics to whetether the APPI has decreased or shown improvement when compared to study participants who did not receive Stimulan during their revision total knee replacement surgery.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • APPI within 28 days of primary TKR
  • Acute hematogenous infection within 4 weeks of symptoms

Exclusion criteria

  • Exposed prosthesis
  • Infection occuring in revised joints
  • Poly articular infections
  • have allergies to tobramycin or Vancomycin
  • previous chronic infections in or around any ipsilateral extremity trauma or implants

Trial design

0 participants in 2 patient groups

APPI of TKR-Stimulan
Description:
Surgery Stimulan beads 2.4 G Tobramycin 2.0 G Vancomycin
Treatment:
Procedure: APPI of TKR-Stimulan
APPI of TKR-historical
Description:
Surgery 2.4 G Tobramycin 2.0 G Vancomycin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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