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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04839783
Other study ID # 20201713
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 7, 2020
Est. completion date July 7, 2032

Study information

Verified date November 2023
Source Spine and Scoliosis Research Associates
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


Description:

The goal of this study is to understand how the difference in positioning of a patient intraoperatively, as part of performing an anterior posterior spine fusion surgery, can affect short term and long term outcomes. This will be accomplished through observational techniques that will not affect the care patients will receive for their spinal conditions. Patients will be asked to complete health and wellness surveys before and after survey to determine how they are doing before surgery and then what if any changes their respective surgeries have had on their lives. Further spine x-rays that they have taken to plan their surgeries and assess their recovery will be measured, when available. X-rays will not be taken only for research purposes. Additionally aspects of their surgeries will be noted such as where hardware is placed and how long different parts of the surgery took. Follow-up is planned to be out to 10 years post-operatively with the goal of collecting information about any revision spine surgeries that would happen during those 10 years as well.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date July 7, 2032
Est. primary completion date July 7, 2030
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion 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 Exclusion Criteria: 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.

Study Design


Locations

Country Name City State
Australia Melbourne Orthopedic Group Windsor Victoria
United States Austin Spine Austin Texas
United States New England Baptist Hospital Boston Massachusetts
United States NYU Langone Health New York New York
United States The Spine Clinic of Oklahoma City Oklahoma City Oklahoma
United States Atlantic Neurosurgical and Spine Specialists Wilmington North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Spine and Scoliosis Research Associates

Countries where clinical trial is conducted

United States,  Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Pain Interference Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Pain Interference. 10 years
Primary Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Pain Intensity Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Pain Intensity. 10 years
Primary Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Depression Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Depression. 10 years
Primary Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Anxiety Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Anxiety. 10 years
Primary Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Physical Function Scores Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates less Physical Function. 10 years
Primary Difference in Radiographic Measurements-Cobb Angles Assess the difference between pre-op and post-op measurements of Cobb Angles using available spinal x-rays for patients whose Cobb Angle was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-Fractional Curve Cobb Angles Assess the difference between pre-op and post-op measurements of Fractional Curve Cobb Angles using available spinal x-rays for patients whose Fractional Curve Cobb Angle was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-C7 Sagittal Vertical Alignment (SVA) Assess the difference between pre-op and post-op measurements of C7 SVA using available spinal x-rays for patients whose C7 SVA was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-Coronal Sagittal Vertical Alignment (SVA) Assess the difference between pre-op and post-op measurements of Coronal SVA using available spinal x-rays for patients whose Coronal SVA was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-Pelvic Incidence (PI) Assess the difference between pre-op and post-op measurements of PI using available spinal x-rays for patients whose PI was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-Pelvic Tilt (PT) Assess the difference between pre-op and post-op measurements of spinal x-rays for patients whose PT was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-Lumbar Lordosis (LL) Assess the difference between pre-op and post-op measurements of spinal x-rays for patients whose LL was to be changed as part of their surgical plan. 10 years
Primary Difference in Radiographic Measurements-T1 Pelvic Angle (TPA) Assess the difference between pre-op and post-op measurements of spinal x-rays, for patients whose TPA was to be changed as part of their surgical plan. 10 years
Primary Revision Incidence Determine the incidence of spine surgery revisions after the initial surgery. 10 years
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