- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05793697
Assessment Of Different Scores In Predicting Outcome In AECOPD Patients In Emergency Department
Assessment Of Different Scores In Predicting Outcome In Acute Exacerbation Of Chronic Obstructive Pulmonary Disease Patients In Emergency Department
Study Overview
Status
Conditions
Detailed Description
Chronic obstructive pulmonary disease (COPD) is one of the top three causes of death worldwide, and 90% of deaths occur in low- and middle-income countries.
Acute exacerbation of chronic obstructive pulmonary disease(AECOPD) is defined as an acute change in patient's dyspnea, cough, or sputum beyond normal variability that is sufficient to warrant a change in therapy. AECOPD has a negative effect on the quality of life, admission and readmission rates, and disease progression.
For these reasons, appropriate management of acute exacerbations is recommended by national and international organizations.
Identifying high-risk dying patients on hospital admission helps in triaging them to the required level of care.
The use of early warning scores in follow-up is recommended for the early detection of critically ill patients and the prediction of clinical deterioration. CURB65, BAP65, qSOFA , DECAF and NEWS, which mainly involve mental status, respiratory rate, oxygen saturations, pulse, blood pressure, age, BUN level, etc., can be used to predict AECOPD-associated mortality in ED given the simple structure and data availability.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: mohamed mo saleh, bachelor
- Phone Number: 01128534859
- Email: drmohamed33333@gmail.com
Study Contact Backup
- Name: maha mo sayed, MD
- Phone Number: 01009656205
- Email: mahaelkholy@yahoo.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patient presented to ED with acute exacerbation of COPD.
Exclusion Criteria:
- Patient presented with acute insult affecting other system.
- Patient transferred to other centers.
- Inadequate data.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluate the value of different scores in predicting hospital mortality
Time Frame: one year
|
Assessment Of Different Scores In Predicting Outcome In Acute Exacerbation Of Chronic Obstructive Pulmonary Disease Patients In Emergency Department as DECAF(dyspnea grade V according to eMRCD,esinopenia<0.05x10*9/L,consolidation,acidemia<7.30,atrial fibrillation) 1=mild,2_3=moderate,4_5=severe can be used to predict AECOPD-associated mortality in ED given the simple structure and data availability. |
one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Value of these scores in predicting need for MV.
Time Frame: one year
|
Value of these scores in predicting need for MV in AECOPD patient in ER
|
one year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: reham mo abdelmonem, MD, Assiut Uneversity
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- different scores in AECOPD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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