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General vs Spinal in Total Joint Arthroplasty (TJA)

NCT06747494 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2396

Last updated 2026-03-18

No results posted yet for this study

Summary

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.

Conditions

Interventions

PROCEDURE

General Anesthesia

Participants will receive a one-time general anesthesia dose during the total joint arthroplasty procedure as per standard of care.

PROCEDURE

Spinal Anesthesia

Participants will receive a one-time spinal anesthesia dose during the total joint arthroplasty procedure as per standard of care.

Sponsors & Collaborators

  • University of Miami

    lead OTHER

Principal Investigators

  • Victor H Hernandez, MD · University of Miami

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-01
Primary Completion
2030-03-01
Completion
2030-03-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06747494 on ClinicalTrials.gov