Patient Specific Talus Spacer Post Approval Study

Part of paid clinical trials in Santa Rosa, California.

Sponsor
Paragon 28
Study ID
NCT05364606
Status
Recruiting

Conditions

  • Avascular Necrosis of the Talus

Eligibility Criteria

Sex
ALL
Age
21 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Patient Specific Talus Spacer — DEVICE
    Patient Specific Talus Spacer is a solid polished replica of the patient's bone.

Study Details

Humanitarian Device Exemption Approved Patient Specific Talus Spacer Post Approval Study.

Key Dates

First listed
May 6, 2022
Start date
Jul 8, 2022
Status verified
Sep 2026
Primary completion
Aug 30, 2033
Completion
Nov 30, 2033

Study Design

Enrollment
50 participants (estimated)

Arms

  • Arm: 50 Subjects
    50 Subjects Receiving the Patient Specific Talus Spacer.

Primary Outcome Measure

Clinically Significant Improvement in Pain on the Visual Analog Scale (VAS) [ Time Frame: At 5 years compared to Baseline ]

Central Contacts

Locations (5)

FacilityCityStateZIPSite coordinators
Sutter Health Santa RosaSanta RosaCalifornia95403
Thomas Chang, DPM
707-544-3400
Thomas Chang, DMP (PRINCIPAL_INVESTIGATOR)
Fort Wayne OrthopedicsFort WayneIndiana46804
Faith Etherington, PA-C
260-436-8686
Matthew Beuchel, MD (PRINCIPAL_INVESTIGATOR)
Mercy Institute for Foot & Ankle ReconstructionBaltimoreMaryland21202
Katherine Convery
410.332.9035
Patrick Maloney, MD (PRINCIPAL_INVESTIGATOR)
Clifford Jeng, MD (SUB_INVESTIGATOR)
Lew Schon, MD (SUB_INVESTIGATOR)
Rebecca Cerrato, MD (SUB_INVESTIGATOR)
Medical University of South CarolinaCharlestonSouth Carolina29425
Hana Hashioka
Christoper Gross, MD (PRINCIPAL_INVESTIGATOR)
Daniel Scott, MD (SUB_INVESTIGATOR)
UT Physicians Orthopedics - PearlandPearlandTexas77584
Jordan Harmon
713-962-9954
Taggart Gauvain, MD (PRINCIPAL_INVESTIGATOR)

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