NCT01979094

Brief Summary

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

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,296

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2013

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2013

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

October 24, 2013

Completed
15 days until next milestone

First Posted

Study publicly available on registry

November 8, 2013

Completed
10.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 4, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 4, 2024

Completed
Last Updated

March 5, 2024

Status Verified

March 1, 2024

Enrollment Period

10.7 years

First QC Date

October 24, 2013

Last Update Submit

March 3, 2024

Conditions

Spine Condition

Outcome Measures

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.

    5 years

Study Arms (1)

spinal arthrodesis and/or arthroplasty procedures

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability 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.

You may qualify if:

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

You may not qualify if:

  • N/A

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Ohio State Unviersity

Columbus, Ohio, 43210, United States

Location

Study Officials

  • H. Francis Farhadi, MD, PhD

    Ohio State University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

October 24, 2013

First Posted

November 8, 2013

Study Start

May 1, 2013

Primary Completion

January 4, 2024

Study Completion

January 4, 2024

Last Updated

March 5, 2024

Record last verified: 2024-03

Locations

US(1)