PCA Administration in Prosthetic Joint Infection

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorDr. Dean Reeves Clinic

About this trial

Determine if dietary protocatechuic acid (PCA) will affect health biomarkers in patient undergoing revision surgery for a knee prosthetic joint infection

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

3 weeks or more after total knee arthroplasty

One or more symptoms of infection, including redness, swelling, pain, increasing range of motion loss, fever, nausea, and loss of appetite.

WBC count of aspirate >50,000 cells per μL

Disqualifiers

Not willing to undergo blood draw at 3 months.

Trial design

Design model

Single group

Treatments tested in this trial

  • Oral PCA

    Dietary supplement

    PCA 1,000 mg BID until surgery, held until anticoagulation, and resumed at 1,000 mg daily for 4 years

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: PCA administratonOther 1 intervention

Trial outcomes

Primary outcomes

1

Change in immunity factor CXCL9 from 0 to 3 months

Time frame
0 and 3 months
2

Change in HbA1c from 0 to 3 months

Time frame
0 and 3 months

Secondary outcomes

1

Reinfection rate after revision for prosthetic joint infection

Time frame
0 to 4 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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

Dr. Dean Reeves Clinic

Lead sponsor

Lanny Johnson, M.D.

Collaborator

Leo Whiteside, M.D.

Collaborator

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