- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03798158
Prevalence and Characterization of Persistent Dyspnea After Hospitalization (DyHP)
July 22, 2021 updated by: Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
Prevalence and Characterization of Persistent Dyspnea After an Hospitalization for a Respiratory Disease
The investigators aim to make an overview of persistent dyspnea at the end of an hospitalization for a respiratory disease using an actual tool, the Multidisciplinary Dyspnea Profile questionnaire.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Paris, France, 75013
- Recruiting
- ADOREPS
-
Contact:
- Capucine MORELOT, MD,PhD
- Phone Number: 0033 01 42 16 77 71
- Email: capucine.morelot@aphp.fr
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Every consecutive patient admitted to hospitalization for a respiratory cause having a significant dyspnea
Description
Inclusion Criteria:
- Age over 18 years old
- Able to respond the questionnaire
- Presenting at admission a dyspnea over 3/10 on numerical analogic scale
- Admitted for a respiratory cause
Exclusion Criteria:
- cognitive impairment
- aphasia
- no french-speaking person
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Prevalence of persistent dyspnea in the end of an hospitalization for a a respiratory disease
Time Frame: An average of one week, until the end of the hospitalization
|
An average of one week, until the end of the hospitalization
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Characterization of persistent dyspnea using MDP
Time Frame: An average of one week, until the end of the hospitalization
|
An average of one week, until the end of the hospitalization
|
|
Outcome of patients with persistent dyspnea after hospitalization
Time Frame: 6 months
|
6 months mortality, incidence of rehospitalization
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
April 11, 2019
Primary Completion (Anticipated)
April 30, 2025
Study Completion (Anticipated)
April 30, 2025
Study Registration Dates
First Submitted
November 21, 2018
First Submitted That Met QC Criteria
January 8, 2019
First Posted (Actual)
January 9, 2019
Study Record Updates
Last Update Posted (Actual)
July 23, 2021
Last Update Submitted That Met QC Criteria
July 22, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018-A02757-48
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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