Please note that the copy function is not enabled for this field.
If you wish to
modify
existing outcomes, please copy and paste the current outcome text into the Update field.
LOGIN
CREATE ACCOUNT
LOGIN
CREATE ACCOUNT
MY TRIALS
REGISTER TRIAL
FAQs
HINTS AND TIPS
DEFINITIONS
Trial Review
The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this
information for consumers
Download to PDF
Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04839783
Registration number
NCT04839783
Ethics application status
Date submitted
10/03/2021
Date registered
9/04/2021
Date last updated
22/11/2023
Titles & IDs
Public title
Single Position Spine Surgery Registry
Query!
Scientific title
Multi-center, Prospective, Single Position, Spine Surgery Outcomes Registry
Query!
Secondary ID [1]
0
0
20201713
Query!
Universal Trial Number (UTN)
Query!
Trial acronym
SPSG Registry
Query!
Linked study record
Query!
Health condition
Health condition(s) or problem(s) studied:
Spine Fusion
0
0
Query!
Spinal Stenosis
0
0
Query!
Degenerative Disc Disease
0
0
Query!
Condition category
Condition code
Musculoskeletal
0
0
0
0
Query!
Other muscular and skeletal disorders
Query!
Neurological
0
0
0
0
Query!
Other neurological disorders
Query!
Intervention/exposure
Study type
Observational [Patient Registry]
Query!
Patient registry
Query!
Target follow-up duration
Query!
Target follow-up type
Query!
Description of intervention(s) / exposure
Query!
Comparator / control treatment
Query!
Control group
Query!
Outcomes
Primary outcome [1]
0
0
Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Pain Interference
Query!
Assessment method [1]
0
0
Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Pain Interference.
Query!
Timepoint [1]
0
0
10 years
Query!
Primary outcome [2]
0
0
Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Pain Intensity
Query!
Assessment method [2]
0
0
Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Pain Intensity.
Query!
Timepoint [2]
0
0
10 years
Query!
Primary outcome [3]
0
0
Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Depression
Query!
Assessment method [3]
0
0
Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Depression.
Query!
Timepoint [3]
0
0
10 years
Query!
Primary outcome [4]
0
0
Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Anxiety
Query!
Assessment method [4]
0
0
Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates more Anxiety.
Query!
Timepoint [4]
0
0
10 years
Query!
Primary outcome [5]
0
0
Difference in Patient-Reported Outcomes Measurement Information System (PROMIS) Domain-Physical Function Scores
Query!
Assessment method [5]
0
0
Assess the difference between pre-op and post-op scores. Scores range from 0-100. A higher number indicates less Physical Function.
Query!
Timepoint [5]
0
0
10 years
Query!
Primary outcome [6]
0
0
Difference in Radiographic Measurements-Cobb Angles
Query!
Assessment method [6]
0
0
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.
Query!
Timepoint [6]
0
0
10 years
Query!
Primary outcome [7]
0
0
Difference in Radiographic Measurements-Fractional Curve Cobb Angles
Query!
Assessment method [7]
0
0
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.
Query!
Timepoint [7]
0
0
10 years
Query!
Primary outcome [8]
0
0
Difference in Radiographic Measurements-C7 Sagittal Vertical Alignment (SVA)
Query!
Assessment method [8]
0
0
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.
Query!
Timepoint [8]
0
0
10 years
Query!
Primary outcome [9]
0
0
Difference in Radiographic Measurements-Coronal Sagittal Vertical Alignment (SVA)
Query!
Assessment method [9]
0
0
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.
Query!
Timepoint [9]
0
0
10 years
Query!
Primary outcome [10]
0
0
Difference in Radiographic Measurements-Pelvic Incidence (PI)
Query!
Assessment method [10]
0
0
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.
Query!
Timepoint [10]
0
0
10 years
Query!
Primary outcome [11]
0
0
Difference in Radiographic Measurements-Pelvic Tilt (PT)
Query!
Assessment method [11]
0
0
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.
Query!
Timepoint [11]
0
0
10 years
Query!
Primary outcome [12]
0
0
Difference in Radiographic Measurements-Lumbar Lordosis (LL)
Query!
Assessment method [12]
0
0
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.
Query!
Timepoint [12]
0
0
10 years
Query!
Primary outcome [13]
0
0
Difference in Radiographic Measurements-T1 Pelvic Angle (TPA)
Query!
Assessment method [13]
0
0
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.
Query!
Timepoint [13]
0
0
10 years
Query!
Primary outcome [14]
0
0
Revision Incidence
Query!
Assessment method [14]
0
0
Determine the incidence of spine surgery revisions after the initial surgery.
Query!
Timepoint [14]
0
0
10 years
Query!
Eligibility
Key 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
Query!
Minimum age
18
Years
Query!
Query!
Maximum age
100
Years
Query!
Query!
Sex
Both males and females
Query!
Can healthy volunteers participate?
No
Query!
Key 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.
Query!
Study design
Purpose
Query!
Duration
Query!
Selection
Query!
Timing
Prospective
Query!
Statistical methods / analysis
Query!
Recruitment
Recruitment status
Recruiting
Query!
Data analysis
Query!
Reason for early stopping/withdrawal
Query!
Other reasons
Query!
Date of first participant enrolment
Anticipated
Query!
Actual
7/07/2020
Query!
Date of last participant enrolment
Anticipated
Query!
Actual
Query!
Date of last data collection
Anticipated
7/07/2032
Query!
Actual
Query!
Sample size
Target
1000
Query!
Accrual to date
Query!
Final
Query!
Recruitment in Australia
Recruitment state(s)
VIC
Query!
Recruitment hospital [1]
0
0
Melbourne Orthopedic Group - Windsor
Query!
Recruitment postcode(s) [1]
0
0
3181 - Windsor
Query!
Recruitment outside Australia
Country [1]
0
0
United States of America
Query!
State/province [1]
0
0
Massachusetts
Query!
Country [2]
0
0
United States of America
Query!
State/province [2]
0
0
New York
Query!
Country [3]
0
0
United States of America
Query!
State/province [3]
0
0
North Carolina
Query!
Country [4]
0
0
United States of America
Query!
State/province [4]
0
0
Oklahoma
Query!
Country [5]
0
0
United States of America
Query!
State/province [5]
0
0
Texas
Query!
Funding & Sponsors
Primary sponsor type
Other
Query!
Name
Spine and Scoliosis Research Associates
Query!
Address
Query!
Country
Query!
Ethics approval
Ethics application status
Query!
Summary
Brief 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.
Query!
Trial website
https://clinicaltrials.gov/study/NCT04839783
Query!
Trial related presentations / publications
Query!
Public notes
Query!
Contacts
Principal investigator
Name
0
0
Query!
Address
0
0
Query!
Country
0
0
Query!
Phone
0
0
Query!
Fax
0
0
Query!
Email
0
0
Query!
Contact person for public queries
Name
0
0
Query!
Address
0
0
Query!
Country
0
0
Query!
Phone
0
0
Query!
Fax
0
0
Query!
Email
0
0
Query!
Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT04839783
Download to PDF