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Completed

NCT Number: NCT02602613

AMENDTM Mitral Valve Repair System, Annuloplasty Ring Applied in a Transcatheter Method

A multi center study to evaluate the safety of the AMENDTM Mitral Valve Repair System and its ability to reduce mitral regurgitation. AMEND device is an annuloplasty ring implanted in a minimally invasive trans-catheter method.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

ZNA Middelheim Hospital, Antwerp, Belgium

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient age ≥18
  • The patient requires mitral valve annuloplasty for mitral regurgitation without the need for concomitant cardiovascular surgical procedures
  • NYHA functional capacity ≥2
  • The subject is high risk to undergo a mitral valve surgery as assessed by the center heart team
  • The patient is willing to comply with study procedures and is available to return to the implant center for follow-up visits.
  • The patient is willing to provide Informed consent

Exclusion criteria

  • Cardiac or non-cardiac major or progressive disease, which in the investigator's discretion produces an unacceptable increased risk to the patient.
  • Life expectancy of less than twelve months.
  • Heavily calcified annulus or leaflets.
  • Previous or active endocarditis.
  • Active infection.
  • A previously implanted prosthetic mitral valve or annuloplasty ring/band.
  • The patient is contraindicated to general anesthesia.
  • Pregnant (urine HCG test result positive) or lactating patient.
  • Drug or alcohol abuse.
  • Participation in concomitant research studies of investigational products that will interfere with the study.

Treatment and study plan

AMEND Mitral Valve Repair System

Device

Annuloplasty ring applied in a transcatheter method

Primary outcomes

  1. Safety - Freedom from major SAE's at 30 days following procedure

    Time frame: 30 days

    Freedom from major SAE's at 30 days following procedure

  2. Technical success of implantation

    Time frame: End of procedure

    Ring location and attachment based on echocardiography

Secondary outcomes

  1. Safety - Freedom from major SAE's at 6 months following procedure

    Time frame: 6 months

    Freedom from major SAE's at 6 months following procedure

Sponsors and collaborators

Lead sponsor

Valcare Medical Ltd.

Industry

Registry information

Official study title

AMEND I Study - for the Valcare Medical AMEND TM Mitral Valve Repair System

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Nov 11, 2015
Registry last updated
May 3, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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