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

> **NCT02452671** · — · TERMINATED · sponsor: **Cartiva, Inc.** · enrollment: 15 (actual)

## Conditions studied

- Toe Joint Deformity

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT02452671
- **Lead sponsor:** Cartiva, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** TERMINATED
- **Start date:** 2015-06
- **Primary completion:** 2017-02
- **Final completion:** 2017-02
- **Target enrollment:** 15 (ACTUAL)
- **Why stopped:** Enrollment temporarily stopped
- **Last updated:** 2017-03-22


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02452671

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02452671, "Observational Plan to Obtain Clinical Experience and Follow up Data on the Use of the ProxiFuse Hammer Toe Device". Retrieved via AI Analytics 2026-06-08 from https://api.ai-analytics.org/clinical/NCT02452671. Licensed CC0.

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