General vs Spinal in Total Joint Arthroplasty (TJA)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Miami

About this trial

The purpose of this research is to compare post-operative outcomes from patients undergoing TJA. The study team wants to learn about outcomes like length of hospital stay, post-operative pain scores, post-operative nausea, deep and superficial surgical site infection, periprosthetic fracture (a broken bone that occurs around an orthopaedic implant), implant dislocation, readmission rates, and revision rates.

Eligibility criteria

Qualifiers

Patients undergoing a primary total hip or knee arthroplasty

Subjects must be capable of providing informed consent

English or Spanish speaking

Disqualifiers

Prior lumbar surgery with hardware insertion

Elevated intracranial pressure

Infection at the site of the procedure

Thrombocytopenia or coagulopathy

Trial design

Treatments tested in this trial

  • General Anesthesia
  • Spinal Anesthesia

Treatment groups

2,396 Participants
are divided into 2 treatment groups

Sponsors and collaborators