- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03772275
Utility of Some Novel Biomarkers of Patients With Chronic Heart Failure
December 8, 2018 updated by: Sherief Abd-Elsalam
Clinical and Economical Study Evaluating the Utility of Some Novel Biomarkers of Patients With Chronic Heart Failure
Clinical and Economic study of some new biomarkers in chronic heart failure.
Study Overview
Status
Recruiting
Conditions
Detailed Description
The study aimed at evaluation of the clinical and economic value of some new biomarkers in chronic heart failure.
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
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
-
-
Elgharbia
-
Tanta, Elgharbia, Egypt, 35111
- Recruiting
- Sherief Abd-Elsalam
-
Contact:
- Nermin W Ishak, Msc
-
-
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 75 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- NYHA-Class II-IV
Exclusion Criteria:
- Liver or renal dysfunction. --DM
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
- Primary Purpose: DIAGNOSTIC
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: New york Heart Association Class II-IV
New york Heart Association Class II-IV heart failure
|
New york Heart Association Class II-IV " study of markers"
Other Names:
|
|
ACTIVE_COMPARATOR: New york Heart Association Class I
New york Heart Association Class I with no heart failure
|
New york Heart Association Class I
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of participants with elevated markers (IL17)
Time Frame: 6 months
|
Number of participants with elevated markers (IL17)
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Osama M Ibrahim, Prof, Prof of Clinical Pharmacy
- Study Director: Medhat M Eshmawy, Prof, Cardiology Department- Tanta University
- Study Chair: Nermin W Ishaq, Msc, Clinical pharmacy Department- Tanta University
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)
October 1, 2018
Primary Completion (ANTICIPATED)
October 1, 2026
Study Completion (ANTICIPATED)
October 1, 2027
Study Registration Dates
First Submitted
December 7, 2018
First Submitted That Met QC Criteria
December 8, 2018
First Posted (ACTUAL)
December 11, 2018
Study Record Updates
Last Update Posted (ACTUAL)
December 11, 2018
Last Update Submitted That Met QC Criteria
December 8, 2018
Last Verified
December 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Heart failure
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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.