# Observational Registry on the HARPOON Device

> **NCT04393779** · NA · TERMINATED · sponsor: **Edwards Lifesciences** · enrollment: 26 (actual)

## Conditions studied

- Severe Degenerative Mitral Regurgitation Due to Mid-segment Posterior Leaflet Prolapse

## Interventions

- **DEVICE:** HARPOON Beating Heart Mitral Valve Repair System (MVRS)

## Key facts

- **NCT ID:** NCT04393779
- **Lead sponsor:** Edwards Lifesciences
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2020-10-02
- **Primary completion:** 2022-11-17
- **Final completion:** 2022-11-17
- **Target enrollment:** 26 (ACTUAL)
- **Why stopped:** Low enrollment
- **Last updated:** 2024-01-29

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04393779

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04393779, "Observational Registry on the HARPOON Device". Retrieved via AI Analytics 2026-06-22 from https://api.ai-analytics.org/clinical/NCT04393779. Licensed CC0.

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