Surgery: Phantom Hindfoot TTC/TC Nail System Post-Market Clinical Follow-Up Study

Summary

This study focuses on individuals who had a surgery 12 or more months ago that included the implantation of the Phantom Hindfoot TTC/TC Nail System. The purpose of this study is to evaluate the safety and helpfulness of the Phantom Hindfoot TTC Nail and the Phantom ActivCore Nail. Safety will be measured by looking at any problems the patient had during or after surgery. Helpfulness will be measured by looking at answers provided about the patient’s pain and quality of life in the study questionnaire.


Inclusion Criteria

Not Available


Study Location(s)

Beverly


Full Title

Phantom® Hindfoot TTC/TC Nail System Post-Market Clinical Follow-Up Study

Details
Disease Type/Condition

Other

Principal Investigator

Thordarson, David

Age Group

Adult

Phase

N/A

IRB Number

STUDY00002287


Contact
Phone
310-423-6252
Email
clinicaltrials@cshs.org
Want to join the study or
learn more?

Details
Disease Type/Condition

Other

Principal Investigator

Thordarson, David

Age Group

Adult

Phase

N/A

IRB Number

P31-SP-0001


Contact
Phone
310-423-6252
Email
clinicaltrials@cshs.org
Want to join the study or
learn more?