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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06015997
Other study ID # ANAC.JO.2023.ATTR.TAVR.ME
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 1, 2023
Est. completion date November 1, 2025

Study information

Verified date August 2023
Source Jordan Collaborating Cardiology Group
Contact Ramzi Tabbalat, MD, FACC
Phone 00962795535522
Email ramzi_md@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

ATTR-cardiac amyloidosis (CA) is present in 4% to 16% of elderly patients with severe calcific aortic stenosis (AS). The reasons for this association are not fully known. It is hypothesized that an amyloidotic infiltration of the aortic valve acts as a trigger for the development of endothelial damage and subsequent calcification. Elderly patients undergoing TAVI will be evaluated for the presence of ATTR-CA in Jordan.


Description:

ATTR-cardiac amyloidosis (CA) is present in 4% to 16% of elderly patients with severe calcific aortic stenosis (AS). The reasons for this association are not fully known. Two hypotheses may explain this association 1. Amyloidotic infiltration of the aortic valve acts as a trigger for the development of endothelial damage and subsequent calcification. 2. The increased myocardial strain induced by AS may locally favor the process of amyloidogenesis and tissue infiltration. Transarterial AV replacement (TAVI) is the treatment of choice for elderly patients with severe calcific AS. Studies have shown a prevalence of about 10% of ATTR cardiac amyloidosis in patients undergoing TAVI. The diagnosis is based on a positive nuclear scan (PYP, DPD or HMDP) and ruling out AL amyloidosis in patients with positive scans. While studies have shown no impact of ATTR on prognosis in TAVI patients, there is evidence of poorer quality of life, increased in-hospital acute ischemic stroke, increased cardiac and heart failure hospitalizations, increased conduction abnormalities, compared to patients without ATTR undergoing TAVI. The prevalence of ATTR in TAVI patients in Jordan and Middle Eastern populations has not been previously evaluated. The purpose of this study is to evaluate the prevalence of ATTR cardiac amyloidosis in elderly Middle Eastern patients undergoing TAVI and to document the clinical characteristics, procedural outcomes and 1 year follow up of such patients compared to patients without ATTR.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date November 1, 2025
Est. primary completion date September 30, 2025
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Age =65 years - Severe aortic stenosis - Patient underwent TAVR procedure - Positive pyruvate PO4 scan Exclusion Criteria: - Diagnosis of AL amyloidosis base on free light chain assay, serum and urine immune electrophoresis.

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Jordan Collaborating Cardiology Group

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of ATTR CA in TAVR patients Consecutive elderly (=65 years) patients who are undergoing TAVI will be included.
Patients will be invited to undergo a pyruvate PO4 (PYP) scan. Patients with positive scans will undergo further testing to rule out AL amyloidosis (Free light chain assay, SIFEP, UIFEP). Data collection will include all pertinent clinical characteristics, peri- procedural details.
On admission ( from time of admission to time of discharge from the hospital) and within 10 days.
Primary Cardiovascular event at One year follow up Events at one year defined as the occurrence of all-cause death, and hospital admission for heart failure or aortic valve reintervention. One year after enrollment: up to 30 days after the passage of 365 days after the TAVR procedure
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