search
Back to results

A Prospective, Multicenter, Single Arm Feasibility Study of the Safety and Performance of GRADION™ Hip Total Cartilage Replacement (TCR)™ in the Treatment of Degenerative Joint Disease of the Hip

Primary Purpose

Degenerative Joint Disease of the Hip

Status
Terminated
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
GRADION™ Hip Total Cartilage Replacement (TCR)™
Sponsored by
Biomimedica, Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Degenerative Joint Disease of the Hip

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary hip surgery for Noninflammatory Degenerative Joint Disease (NIDJD) such as osteo/degenerative arthritis, and is indicated for cartilage replacement
  • Skeletally mature or at least 18 years of age and has normal anatomy
  • Patient signs the Informed Consent form
  • Failed medical management
  • There will be size limitations on patients also - available size range is 46mm-54mm.

Exclusion Criteria:

  • Allergic to polyether urethane, sodium polyacrylate, bone cement or any of its components
  • Previous fusion, acute femoral neck fracture and/or above knee amputation
  • Revision of any previous hip procedure
  • Slipped capital femoral epiphysis (SCFE)
  • Rheumatoid arthritis
  • AVN

Sites / Locations

  • Rijnstate Arnhem

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

GRADION™ Hip Total Cartilage Replacement (TCR)™

Arm Description

Outcomes

Primary Outcome Measures

Adverse events

Secondary Outcome Measures

Full Information

First Posted
November 1, 2013
Last Updated
May 16, 2016
Sponsor
Biomimedica, Inc
search

1. Study Identification

Unique Protocol Identification Number
NCT01982266
Brief Title
A Prospective, Multicenter, Single Arm Feasibility Study of the Safety and Performance of GRADION™ Hip Total Cartilage Replacement (TCR)™ in the Treatment of Degenerative Joint Disease of the Hip
Official Title
A Prospective, Multicenter, Single Arm Feasibility Study of the Safety and Performance of GRADION™ Hip Total Cartilage Replacement (TCR)™ in the Treatment of Degenerative Joint Disease of the Hip
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Terminated
Why Stopped
Device failure
Study Start Date
November 2013 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Biomimedica, Inc

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a prospective, multicenter, single arm feasibility study of the safety and performance of the GRADION™ Hip Total Cartilage Replacement (TCR)™ in patients who require cartilage replacement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Degenerative Joint Disease of the Hip

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GRADION™ Hip Total Cartilage Replacement (TCR)™
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
GRADION™ Hip Total Cartilage Replacement (TCR)™
Primary Outcome Measure Information:
Title
Adverse events
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary hip surgery for Noninflammatory Degenerative Joint Disease (NIDJD) such as osteo/degenerative arthritis, and is indicated for cartilage replacement Skeletally mature or at least 18 years of age and has normal anatomy Patient signs the Informed Consent form Failed medical management There will be size limitations on patients also - available size range is 46mm-54mm. Exclusion Criteria: Allergic to polyether urethane, sodium polyacrylate, bone cement or any of its components Previous fusion, acute femoral neck fracture and/or above knee amputation Revision of any previous hip procedure Slipped capital femoral epiphysis (SCFE) Rheumatoid arthritis AVN
Facility Information:
Facility Name
Rijnstate Arnhem
City
Arnhem
ZIP/Postal Code
6815
Country
Netherlands

12. IPD Sharing Statement

Learn more about this trial

A Prospective, Multicenter, Single Arm Feasibility Study of the Safety and Performance of GRADION™ Hip Total Cartilage Replacement (TCR)™ in the Treatment of Degenerative Joint Disease of the Hip

We'll reach out to this number within 24 hrs