Osteoarthritis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are having their first total hip or knee replacement surgery
- People who are able to understand and agree to participate in the study (give informed consent)
- People who speak English or Spanish
Who may not be able to join:
- People who have had previous lower back surgery that involved inserting metal hardware
- People with increased pressure inside the skull
- People who have an infection at the location where spinal anaesthesia would be given
- People with a low platelet count or problems with blood clotting
- People with severe narrowing of the mitral or aortic heart valves, or a blockage of blood flow out of the left side of the heart
- People with serious spine conditions (such as spinal stenosis, slipped vertebrae, or spine degeneration) that cause nerve pain or difficulty walking due to nerve involvement
- People with a pre-existing neurological (nervous system) disease
- People with heart failure
- People who are unwilling or unable to agree to participate in the study
- Women who are currently pregnant, who are planning to become pregnant in the next year, who think they might be pregnant, or who become pregnant during the study
- People who are currently imprisoned
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Victor H Hernandez, MD, University of Miami
Phone: 305-689-5195
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Length of hospital stay; Change in Patient Pain Scores as measured by the Numeric Rating Pain Scale; Change in Patient Nausea Scores as measured by the Conditioning Scoring Criteria; Prosthetic joint infection; Superficial surgical site infection; Number of periprosthetic fracture; Number of implant dislocation.; Number of participants who are readmitted 90 days after surgery.; Number of participants who receive revision surgery 90 days after surgery.; Number of participant deaths.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.