RECRUITING

General vs Spinal in Total Joint Arthroplasty (TJA)

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Conditions

Knee OsteoarthritisHip OsteoarthritisTotal joint arthroplastyGeneral anesthesiaSpinal anesthesia

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

General Versus Spinal Anesthesia for Total Joint Arthroplasty: A Prospective Randomized Trial

Quick Facts

Study Start:2025-02-01
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06747494

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients undergoing a primary total hip or knee arthroplasty
  2. * Subjects must be capable of providing informed consent
  3. * English or Spanish speaking
  1. * Prior lumbar surgery with hardware insertion
  2. * Elevated intracranial pressure
  3. * Infection at the site of the procedure
  4. * Thrombocytopenia or coagulopathy
  5. * Severe mitral and aortic stenosis and left ventricular outflow obstruction
  6. * Severe spine pathology (spinal stenosis, spondylolisthesis, spondylosis) with radiculopathy and/or neurogenic claudication
  7. * Preexisting neurological disease
  8. * Congestive heart failure
  9. * Severe aortic stenosis
  10. * Patient is unable/unwilling to consent
  11. * 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.
  12. * Prisoners

Contacts and Locations

Study Contact

Victor H Hernandez, MD
CONTACT
305-689-5195
vhh1@med.miami.edu
Antonio M Fernandez-Perez, MS
CONTACT
305-689-5195
axf2089@miami.edu

Principal Investigator

Victor H Hernandez, MD
PRINCIPAL_INVESTIGATOR
University of Miami

Study Locations (Sites)

University of Miami
Miami, Florida, 33136
United States

Collaborators and Investigators

Sponsor: University of Miami

  • Victor H Hernandez, MD, PRINCIPAL_INVESTIGATOR, University of Miami

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-02-01
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2025-02-01
Study Completion Date2026-03-01

Terms related to this study

Keywords Provided by Researchers

  • Total joint arthroplasty
  • General anesthesia
  • Spinal anesthesia

Additional Relevant MeSH Terms

  • Knee Osteoarthritis
  • Hip Osteoarthritis