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Terminated No phase listed Observational

Observational Plan to Obtain Clinical Experience and Follow up Data on the Use of the ProxiFuse Hammer Toe Device

ClinicalTrials.gov ID: NCT02452671

Public ClinicalTrials.gov record NCT02452671. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 3:42 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Observational Plan Designed to Obtain Clinical Experience and Follow up Data on the Use of the ProxiFuse Hammer Toe Device for the Fixation of Osteotomies and Reconstruction of the Lesser Toes Following Correction Procedures

Study identification

NCT ID
NCT02452671
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Cartiva, Inc.
Industry
Enrollment
15 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2015
Primary completion
Jan 31, 2017
Completion
Jan 31, 2017
Last update posted
Mar 21, 2017

2015 – 2017

United States locations

U.S. sites
5
U.S. states
5
U.S. cities
5
Facility City State ZIP Site status
Stanford University Redwood City California 94063
University of Colorado Aurora Colorado 80045
Massachusetts General Hospital Boston Massachusetts 02114
Orthopaedic Associates of Michigan, PC Grand Rapids Michigan 49525
University of Rochester Medical Center Rochester New York 14642

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02452671, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 21, 2017 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02452671 live on ClinicalTrials.gov.

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