- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04089826
Long Term Oxygen Therapy in Patients With Interstitial Lung Disease
September 12, 2019 updated by: Asmaa Mahmoud Mohammed Eltayeb, Assiut University
Role of LTOT in Pateints With ILD
Study the effect of using long term oxygen therapy in patients with interstitial lung disease and chronic hypoxia
Study Overview
Status
Unknown
Detailed Description
long term oxygen can be used in patients with interstitial lung disease with hypoxia and the aim of this study is to k ow whether this will improve life style , exercise tolerance in those patients
Study Type
Observational
Enrollment (Anticipated)
10
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
- Name: Asmaa Mahmoud Mohamed Eltayeb
- Phone Number: 01114203879
- Email: asmaaeltayeb34@gmail.com
Study Contact Backup
- Name: Atef Farouk Elqarn
- Phone Number: 01006474200
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 to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
patients with ILDs who are prescribed for LTOT between eighteen and seventy years old
Description
Inclusion Criteria :
- patients with ILD and hypoxia with SO2<88 at room air and PO2 < or equal 7.3k.pa or < or equal 8 k.pa in presence of lower limb edema , pulmonary hypertension or polycythemia
- age group 18 : 70
Exclusion Criteria :
- Causes of chronic respiratory failure other than ILD.
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dyspnea score improvement
Time Frame: Baseline
|
dyspnea by Modified Medical Research Counsel
|
Baseline
|
Quality of life improvement
Time Frame: Baseline
|
Quality of life by st.George questionnaire
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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.
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 (Anticipated)
September 1, 2019
Primary Completion (Anticipated)
September 1, 2020
Study Completion (Anticipated)
October 1, 2020
Study Registration Dates
First Submitted
September 10, 2019
First Submitted That Met QC Criteria
September 12, 2019
First Posted (Actual)
September 13, 2019
Study Record Updates
Last Update Posted (Actual)
September 16, 2019
Last Update Submitted That Met QC Criteria
September 12, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Role of LTOT in Pateints e ILD
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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