RECRUITING

Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion

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

This is a multi-center, consecutive enrollment registry study to evaluate patient satisfaction post SI Fusion with the TransLoc 3D SI Fusion System.

Official Title

A Multi-Center, Real World Prospective/Retrospective Registry to Evaluate Patient Satisfaction With the TransLoc 3D SI Joint Fusion System

Quick Facts

Study Start:2024-08-15
Study Completion:2024-12-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06487936

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. * Age 18 year or older
  2. * Confirmed Implant of the Transloc 3D Fusion System
  3. * Did not have Transloc device removed or another manufacturer device implanted post Transloc
  4. * Does not have other manufacturer's titanium or metal implant
  5. * Patient may be included with prior allograft implant
  6. * Willing to participate and give written consent
  7. * Must have or planned CT post ≥1 year per standard of care
  1. * Patient is younger than 18 years
  2. * Patient is unable to sign the Informed Consent
  3. * Implant of other manufacturer's titanium or alternative metal implant
  4. * Revision with another manufacturer's implant
  5. * Fracture or unresolved trauma of implant side after implantation of TransLoc
  6. * Patient unwilling to participate in Patient Satisfaction Survey
  7. * Patient has not returned for Standard of Care follow-up

Contacts and Locations

Study Contact

Carley Wiegner
CONTACT
888-743-8736
carley@cornerloc.com
Bob Compton
CONTACT
bob@cornerloc.com

Principal Investigator

Lee James, DO
PRINCIPAL_INVESTIGATOR
Advanced Orthopedic Center

Study Locations (Sites)

Advanced Orthopedic Center
Port Charlotte, Florida, 33948
United States

Collaborators and Investigators

Sponsor: CornerLoc

  • Lee James, DO, PRINCIPAL_INVESTIGATOR, Advanced Orthopedic Center

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 Date2024-08-15
Study Completion Date2024-12-15

Study Record Updates

Study Start Date2024-08-15
Study Completion Date2024-12-15

Terms related to this study

Additional Relevant MeSH Terms

  • Sacroiliac Joint Dysfunction
  • Sacroiliac; Fusion