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Compares treatment options for Knee Osteoarthritis
Official title General vs Spinal in Total Joint Arthroplasty (TJA)
ClinicalTrials.gov ID: NCT06747494
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Patients undergoing a primary total hip or knee arthroplasty
- people must be capable of providing informed consent
- English or Spanish speaking
You likely can't join if
- Patients with contraindications for spinal anesthesia such as:
- Prior lumbar surgery with hardware insertion
- Elevated intracranial pressure
- Infection at the site of the procedure
- Thrombocytopenia or coagulopathy
- Severe mitral and aortic stenosis and left ventricular outflow obstruction
See the full eligibility criteria
- Patients undergoing a primary total hip or knee arthroplasty
- people must be capable of providing informed consent
- English or Spanish speaking
- Patients with contraindications for spinal anesthesia such as:
- Prior lumbar surgery with hardware insertion
- Elevated intracranial pressure
- Infection at the site of the procedure
- Thrombocytopenia or coagulopathy
- Severe mitral and aortic stenosis and left ventricular outflow obstruction
- Severe spine pathology (spinal stenosis, spondylolisthesis, spondylosis) with radiculopathy and/or neurogenic claudication
- Preexisting neurological disease Patients with contraindications for general anesthesia such as:
- Congestive heart failure
- Severe aortic stenosis
- Patient is unable/unwilling to consent
- Current pregnancy or women planning on becoming pregnant in the next year, and women who think they might be pregnant, or women who become pregnant during the study period will be removed from the study.
- Prisoners
The study team makes the final eligibility decision.
Where it's taking place
- Miami, Florida, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Miami, Florida, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.