Podocan and Wnt Pathway in Left Ventricular Remodeling of Aortic Stenosis
NCT ID: NCT02624934
Last Updated: 2020-07-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
9 participants
OBSERVATIONAL
2015-10-31
2020-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prospective Balloon Aortic Valvuloplasty
NCT02122900
Branched Thoracic Endovascular Grafts for the Treatment of Thoraco-abdominal Aortic
NCT01874197
BIOVALVE - I / II Clincial Investigation
NCT02249000
Self-Centering Guide Catheter Feasibility Study
NCT02639494
CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat Patients With Severe Aortic Stenosis.
NCT03752866
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
It is expected that 100 participants will be enrolled in the study over 24 months. This is sample size was agreed upon after discussion with the statistics team.
Patients who agree to participate will provide informed consent prior to their cardiac MRI. A 6 minute walk test to measure baseline functional status will be done after consent, preferably just prior to reporting to the MRI suite for their scheduled test. Standard cardiac MRI will be obtained. All patients having a cardiac MRI have an IV line placed as normal procedure. When the line has been placed, prior to contrast infusion (if applicable)or other medication administration, blood samples will be collected to test for circulatory Podocan and Wnt pathway molecules. Approximately 20 cc will be drawn in total. All specimens will be sent to the experimental lab of Dr. Paul Klotman at Baylor Medical Center. All of the Podocan \& Wnt pathway effectory molecules assays will be completed by Dr. Klotman's lab.
The following measurements will be collected from the cardiac MRI:
LV end diastolic (ED) volume: ml LV ED index: ml/m2 LV end systolic (ES) volume: ml LV ES index: ml/m2 LV ejection fraction (EF): % LV Stroke Volume: ml LV Stroke Index: ml/m2 LV Cardiac Output: L/min LV Cardiac Index: L/min/M2 LV Mass: g LV Mass index: g/m2
At 12 months post procedure the following information will be collected from the participants' charts for endpoint analysis:
All cause mortality Cardiac mortality Hospital admissions for valvular disease related clinical events such as congestive heart failure, angina, syncope Valve replacement surgery
Patients who do undergo valve replacement surgery during the 12 month follow up period and are scheduled to undergo a post-op follow up cardiac MRI (expected to be at 9-12 months post-op) will be asked to provide additional blood samples to test for circulatory Podocan and Wnt pathway molecules at the time of the MRI.
Each participant's chart will be reviewed at the time of enrollment and the following variables will be abstracted from the medical record:
age, gender, ethnicity, Most recent Ht, Wt, BP, Heart Rate BMI Tobacco use/history Alcohol use/ history Comorbidities
* Hypertension
* Hyperlipidemia
* Diabetes
* Chronic Kidney Disease
* Cancer
* CAD
Info from previous echocardiogram:
* Ejection fraction
* Valve area
* Gradient
Info from previous cardiac cath (if done):
* Presence/absence of coronary stenosis
* Location \& degree of stenosis
* Aortic valve area
* Calculation of valve area
Info from previous ECG:
* Rhythm
* Left Ventricular Hypertrophy Medications
Laboratory data:
* Lipids
* Chemistries
* Complete Blood Count
* Hemoglobin A1C
* Troponin
* B-type Natriuretic Peptide
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Scheduled for Cardiac MRI
* Patients with known aortic valve area of less than 1 cm² on echocardiogram
* Able to provide informed consent
* Ambulatory and expected to be able to complete 6 minute walk test
Exclusion Criteria
* Unable to complete 6 minute walk test (ex. Wheelchair bound)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Baylor University
OTHER
Bassett Healthcare
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Daniel Katz
Attending Physician - Cardiology
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
D Katz, MD
Role: PRINCIPAL_INVESTIGATOR
Bassett Healthcare
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Bassett Healthcare Network
Cooperstown, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.