PMCFU of an Annular Closure System

Purpose

The purpose of this retrospective chart review study is to collect the data that will be used to provide clinical evidence to support the post-market surveillance program.

Condition

  • Lumbar Disc Herniation

Eligibility

Eligible Ages
All ages
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Records for any subject treated with a Barricaid annular closure device will be considered for inclusion into the study

Exclusion Criteria

  • Records for any subject treated without a Barricaid annular closure device will be considered for exclusion

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Arm Groups

ArmDescriptionAssigned Intervention
Discectomy + annular closure All patients treated with lumbar discectomy and implantation of an annular closure device
  • Device: Annular closure
    Lumbar discectomy patients treated with Annular Closure Device BARRICAID

Recruiting Locations

Orthopedic Institute of Western Kentucy
Paducah, Kentucky 42001
Contact:
Rebekah Vinson
270-442-9461
RVinson@orthopaedicinstitute.com

More Details

NCT ID
NCT05467072
Status
Recruiting
Sponsor
Intrinsic Therapeutics

Study Contact

Kelsey A Miller-Torchia, BA
7819320222
kmiller@in-thera.com

Detailed Description

Retrospective chart review of patients treated with lumbar discectomy and annular closure. Review of patient charts through 3 month post op, for analysis of symptomatic lumbar reherniation at the index level.