Prospective Cohort of Respiratory Insufficiency Outcome (RIO)

September 10, 2010 updated by: University Hospital, Grenoble

Prospective Cohort of Patients With Chronic Obstructive Pulmonary Disease (COPD) Undergoing Domiciliary Noninvasive Positive Pressure Ventilation

The Respiratory Insufficiency Outcome (RIO) project consists in a french multicenter prospective cohort of patients with chronic obstructive pulmonary disease (COPD) undergoing domiciliary noninvasive positive pressure ventilation.

Study Overview

Status

Unknown

Conditions

Study Type

Observational

Enrollment (Anticipated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • France
      • Grenoble, France
        • Recruiting
        • University Hospital
        • Contact:
        • Principal Investigator:
          • JEAN LOUIS PEPIN, PhD
        • Sub-Investigator:
          • CHRISTOPHE PISON, PhD
        • Sub-Investigator:
          • JEAN CHRISTIAN BOREL, PhD
        • Sub-Investigator:
          • ISABELLE PIN, MD
      • Lyon, France
        • Not yet recruiting
        • Hopital de La Croix Rousse
        • Principal Investigator:
          • PASCALE NESME MEYER, MD
      • Paris, France
        • Not yet recruiting
        • Hopital de la Pitie Salpetriere
        • Principal Investigator:
          • THOMAS SIMILOWSKI, PhD
        • Sub-Investigator:
          • JESUS GONZALEZ BERMEJO, MD
      • Saint Etienne, France
        • Not yet recruiting
        • Hopital Nord
        • Principal Investigator:
          • ISABELLE COURT FORTUNE, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

COPD patients undergoing domiciliary noninvasive ventilation

Description

Inclusion Criteria:

  • clinical diagnosis of COPD
  • domiciliary noninvasive ventilation

Exclusion Criteria:

  • noninvasive ventilation set up for a neuromuscular disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Grenoble

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

December 1, 2008

Study Registration Dates

First Submitted

August 30, 2010

First Submitted That Met QC Criteria

August 31, 2010

First Posted (ESTIMATE)

September 1, 2010

Study Record Updates

Last Update Posted (ESTIMATE)

September 13, 2010

Last Update Submitted That Met QC Criteria

September 10, 2010

Last Verified

September 1, 2010

More Information

Terms related to this study

Other Study ID Numbers

  • 08SC01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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