Or v IV Antibiotics for Infection

Joint Infection Clinical Trial

Official title:

Oral vs Intravenous Antibiotics for Treatment of Periprosthetic Joint Infection

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT04723940
• Other study ID #: JPAR 20D.1085
• Status: Enrolling by invitation
• Phase: Phase 3
• Start date: January 25, 2021
• Est. completion date: January 25, 2023

Study information

• Verified date: January 2021
• Source: Rothman Institute Orthopaedics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Management of periprosthetic joint infection (PJI) commonly includes 6 weeks of intravenous (IV) antibiotics after surgical treatment. However, there is little evidence to suggest that oral (PO) therapy results in worse outcomes. This study aims to determine whether or not PO antibiotics are non-inferior to IV antibiotics in treating PJI. The study is a multicenter, parallel-group, randomized (1 : 1), open-label, non-inferiority trial. The non-inferiority margin will be set at 10%. Adults with a clinical diagnosis of PJI according to the International Consensus Meeting (ICM) criteria who would ordinarily receive at least 6 weeks of antibiotics and have received ≤ 7 days of IV therapy from surgery will be included. A total of 308 participants will be centrally computer-randomized to PO or IV antibiotics to complete the first 6 weeks of therapy. Follow-on PO therapy will be permitted in either arm. The primary outcome is the proportion of participants experiencing treatment failure within 1 year. An associated cost-effectiveness evaluation including complications, resource utilization and quality-of-life data will be performed.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 308
• Est. completion date: January 25, 2023
• Est. primary completion date: January 25, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• aged = 18 years
• willing and able to give informed consent
• primary THA or TKA diagnosed with PJI based on International Consensus Meeting criteria

1. A sinus communicating with the prosthesis OR

2. Two positive cultures obtained from the prosthesis OR

3. 3 of 5 criteria:

• Elevated ESR (>30mm/hr) and CRP (>10mg/L)
• Elevated synovial leukocyte count (>3000 cells/µL) or change of ++ on leukocyte esterase strip
• Elevated synovial neutrophil percentage (>80%)
• One positive culture
• Positive histological analysis of periprosthetic tissue (>5 neutrophils per high power field in 5 high power fields x400)
• PJI treated by debridement and implant retention, or excision of the prosthetic joint (with or without planned reimplantation)
• received = 7 days of IV therapy after an appropriate surgical intervention

Exclusion Criteria:

• Previously treated for native septic arthritis or PJI in the same joint
• S. aureus bacteremia on presentation or within the previous month
• clinical, histological or microbiological evidence of mycobacterial, fungal or parasitic etiology of the infection
• any other concomitant infection that, in the opinion of the clinician responsible for the patient, requires a prolonged course of IV antibiotic therapy (e.g. bacterial endocarditis, mediastinal infection, central nervous system infection)
• septic shock or systemic features that, in the opinion of the clinician responsible for the patient, requires a course of IV antibiotic therapy (the patient could be re-evaluated if these features resolved)
• an infection for which there are no suitable antibiotic choices to permit randomization between the two arms of the trial (e.g. when organisms are only sensitive to IV antibiotics or PO antibiotics)
• unlikely to comply with trial requirements following randomization in the opinion of the investigator

Related Conditions & MeSH terms

• Communicable Diseases
• Infection
• Joint Infection

Intervention

Drug:
• Bactrim
Bactrim will be given for 6 weeks to treat joint infection
• Cefadroxil
Cefadroxil will be given for 6 weeks to treat joint infection
• Doxycycline Hcl
Doxycycline HCl will given for 6 weeks to treat joint infection
• Clindamycin
Clindamycin will given for 6 weeks to treat joint infection

Locations

Country	Name	City	State
United States	Rothman Orthopaedic Institute	Philadelphia	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Rothman Institute Orthopaedics

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of Postoperative Infections	The investigator will measure the incidence of postoperative infections in participants treated with oral antibiotics versus those treated with intravenous antibiotics	2 years