European Home Mechanical Ventilation Registry

NCT02315339 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 37

Last updated 2020-04-09

No results posted yet for this study

Summary

The European Home Mechanical Ventilation Registry (EHMVR) will enable a thorough evaluation of HMV by documenting the characteristics of HMV patients and their treatment. This will facilitate a prospective, observational study to identify the primary indications for HMV, describe patterns of HMV use in European countries, and characterize changes in the initiation and utilization of HMV over time. The registry will target all adult individuals who have an indication for HMV. In the EHMVR, patient data from routine clinical care will be documented using an electronic case report form (eCRF). The eCRF will record: patient demographic data; diagnostic information (including primary diagnosis, 6-minute walk time, the presence of depression, and quality of life); blood gases; ventilation treatment (including type of ventilator, modes and settings, interfaces used); follow-up data (including failure rates, side effects, technical issues). An initial Pilot Phase will be launched with the aim to enrol at least 200 patients over a 6-month period to determine the feasibility of the registry. Steering committee members and their institutions will be the main participants in the Pilot Phase. After completion of the Pilot Phase, the registry will be expanded across Europe with the goal of enrolling approximately 10,000 patients over 5 years.

Conditions

Sponsors & Collaborators

  • Clinical Trial Center North Hamburg Germany

    collaborator UNKNOWN
  • CRI-The Clinical Research Institute GmbH

    collaborator INDUSTRY
  • ResMed

    lead INDUSTRY

Principal Investigators

  • Jean-Louis Pepin, Pr · Laboratoire d'EFCR, RDC Haut Chartreuse, CHU Michallon 38043,Grenoble, France

  • Stefano Nava, Pr · Pneumologia e Terapia Intensiva Respiratoria Ospedale Sant' Orsola Malpighi, Italy

  • Anita Simonds, Pr · NIHR Respiratory Biomedical Research Unit, Royal Brompton and Harefield NHS Foundation Trust, United Kingdom

  • Wolfram Windisch, Pr · Lungen Klinik - Chefarzt Abt. Pneumologie Kliniken der StadtKölng GmbH, Ostmerheimer Strasse 200, Germany

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2019-01-31
Completion
2019-01-31

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02315339 on ClinicalTrials.gov