TERMINATED

Single Position Spine Surgery Registry

Conditions

Spine Fusion Spinal Stenosis Degenerative Disc Disease

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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 study is to systematically, prospectively compare surgical fusion techniques for thoracolumbar spinal fusion patients and assess long-term patient outcomes and revision rates following surgery.

Official Title

Multi-center, Prospective, Single Position, Spine Surgery Outcomes Registry

Quick Facts

Study Start:2020-07-07

Study Completion:2025-07-07

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:TERMINATED

Study ID

NCT04839783

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 to 100 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Age greater than or equal to 18 years 2. Ability to speak and read comfortably in English 3. Affliction by a spinal condition warranting evaluation for operative treatment	1. Current incarceration 2. Individuals incapable of consenting and/or objectively responding to surveys, irrespective of reasonable assistance 3. Women currently pregnant or expecting to become pregnant in the near future 4. Subjects participating in another research study, whose protocol would conflict with comprehensive participation in this study 5. Subjects with psychiatric pathology which may impair judgement or the ability to give informed consent.

Inclusion Criteria

Exclusion Criteria

1. Age greater than or equal to 18 years
2. Ability to speak and read comfortably in English
3. Affliction by a spinal condition warranting evaluation for operative treatment

1. Current incarceration
2. Individuals incapable of consenting and/or objectively responding to surveys, irrespective of reasonable assistance
3. Women currently pregnant or expecting to become pregnant in the near future
4. Subjects participating in another research study, whose protocol would conflict with comprehensive participation in this study
5. Subjects with psychiatric pathology which may impair judgement or the ability to give informed consent.

Contacts and Locations

Study Locations (Sites)

New England Baptist Hospital

Boston, Massachusetts, 02120

United States

NYU Langone Health

New York, New York, 10016

United States

Atlantic Neurosurgical and Spine Specialists

Wilmington, North Carolina, 28401

United States

The Spine Clinic of Oklahoma City

Oklahoma City, Oklahoma, 73114

United States

Austin Spine

Austin, Texas, 78626

United States

Collaborators and Investigators

Sponsor: Spine and Scoliosis Research Associates

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 Date2020-07-07

Study Completion Date2025-07-07

Study Record Updates

Study Start Date2020-07-07

Study Completion Date2025-07-07

Terms related to this study

Additional Relevant MeSH Terms

Spine Fusion
Spinal Stenosis
Degenerative Disc Disease