- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04915235
Prevalence and Prognosis of Cardiac Amiloidosis in Turkey (PAPCAT)
May 31, 2021 updated by: Turkish Society of Cardiology
Prevalence and Prognosis of Cardiac Amiloidosis in Turkey- Registry Study
Patients with left ventricular hypertrophy are further examined according to an algorithm to check if they have a cardiac amyloidosis
Study Overview
Study Type
Observational
Enrollment (Anticipated)
2087
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: Ilkay Gucuk, MD
- Phone Number: 902122211738
- Email: tkd@tkd.org.tr
Study Locations
-
-
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Izmir, Turkey
- Recruiting
- Dokuz Eylul University Faculty of Medicine
-
Contact:
- Ebru Ozpelit, 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
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients with left ventricular hypertrophy
Description
Inclusion Criteria:
- Patients with left ventricular hypertrophy without left ventricular pressure or volume (IVS≥13mm)
- Patients with left ventricular hypertrophy and hypertension or aortic stenosis without left ventricular pressure or volume (IVS>15mm)
Exclusion Criteria:
- Patients with left ventricular pressure or volume except the ones with aortic stenosis and arterial hypertension
- Patients with sigmoid septum and their hypertrophy limited in sigmoid area
- Patients with highly probable sarcometric hypertrophy cardiomyopathy confirmed with LV morhpology and genetic testing
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 |
Measure Description |
Time Frame |
---|---|---|
Cardiac Amyloidosis
Time Frame: Upon screening
|
Patients with left ventricular hypertrophy and Cardiac Amyloidosis
|
Upon screening
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
September 18, 2020
Primary Completion (ANTICIPATED)
December 31, 2025
Study Completion (ANTICIPATED)
December 31, 2025
Study Registration Dates
First Submitted
May 31, 2021
First Submitted That Met QC Criteria
May 31, 2021
First Posted (ACTUAL)
June 7, 2021
Study Record Updates
Last Update Posted (ACTUAL)
June 7, 2021
Last Update Submitted That Met QC Criteria
May 31, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PAPCAT
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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