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TerminatedNCT01979094Updated Mar 5, 2024

Spinal Arthrodesis and Spinal Arthroplasty Database Study

An observational study in Spine Condition, sponsored by Stephanus Viljoen. Terminated at 1 site in United States. Per ClinicalTrials.gov, last updated 2024-03-05.

Sponsored by Stephanus Viljoen · Observational

Why this study was terminated
Process changes. New data base will be activated
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
1,296
Sex
All
01

Study summary

To collect and organize data into a repository for future research.

Read the detailed description

To collect and organize data into a repository from the Principal Investigator's (H. Francis Farhadi, MD, PhD) patients who are undergoing spinal arthrodesis and/or spinal arthroplasty procedures at Ohio State University for future research, as yet to be identified. This comprehensive database of patients will allow for gathering of relevant information for potential future research use.

02

Conditions studied

  • Spine Condition
03

In context

Lead sponsor

This is the only study on the registry with Stephanus Viljoen as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Spinal arthrodesis and/or spinal arthroplasty can be performed through either anterior, posterior, or lateral approaches for a variety of traumatic, degenerative, or deformity conditions.

Inclusion criteria

  • Must have had or will undergo a spinal arthrodesis and/or spinal arthroplasty procedure at Ohio State University

Exclusion criteria

Exclusion Criteria:

  • N/A
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
1,296 participants (actual)
Patient registry
No

Groups and cohorts

  • spinal arthrodesis and/or arthroplasty procedures
06

What researchers measure

Primary outcomes

  1. clinical prospective review- Prospective Database study for future studies

    Collecting clinical measurements. Examples of these clinical measurements are the VAS Pain Scale, SF-36, NDI, and ODI.

    Time frame: 5 years

07

Study locations

1 site
  • The Ohio State Unviersity
    Columbus, Ohio 43210, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01979094
Lead sponsor
Stephanus Viljoen
Responsible party
Stephanus Viljoen (Assistant Professor, Ohio State University) — Sponsor-investigator
First posted
Nov 8, 2013
Start date
May 2013
Primary completion
Jan 4, 2024
Completion
Jan 4, 2024
Last update
Mar 5, 2024

Study contacts

H. Francis Farhadi, MD, PhD
principal investigator · Ohio State University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.

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