Novel Echocardiographic and Invasive Haemodynamic Measurements in the Assessment of Patients Low Flow Low Gradient Aortic Stenosis Undergoing TAVI

Cardiovascular Abnormalities Clinical Trial

— LFLG  

Official title:

Utility of Novel Echocardiographic and Invasive Haemodynamic Measurements in the Assessment of Patients Low Flow Low Gradient Aortic Stenosis Undergoing TAVI

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05196815
• Other study ID #: 2021CAR121
• Status: Completed
• Phase: N/A
• Start date: July 1, 2022
• Est. completion date: March 1, 2024

Study information

• Verified date: March 2024
• Source: The Royal Wolverhampton Hospitals NHS Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this study the investigators will assess a variety of novel markers of heart strength (contractility) and assess whether they can give a clearer indication of how well patients with weak hearts respond to the TAVI procedure. The investigators will perform a stress echocardiogram prior to each TAVI procedure and measure the global longitudinal strain (GLS) in the left ventricle (LV) heart muscle, a detailed marker of muscle strength. The investigators will then proceed to the TAVI procedure and measure the contractility of the main pumping chamber in the heart before and after giving a very low dose of an adrenaline -like drug (dobutamine). The patient will already have received this short acting drug (at the same and higher doses) during their routine care planning stress echocardiogram.

Description:

In this study the investigators will assess a variety of novel markers of heart strength (contractility) and assess whether they can give a clearer indication of how well patients with weak hearts respond to the TAVI procedure. The investigators will perform a stress echocardiogram prior to each TAVI procedure and measure the global longitudinal strain (GLS) in the left ventricle (LV) heart muscle, a detailed marker of muscle strength. The investigators will then proceed to the TAVI procedure and measure the contractility of the main pumping chamber in the heart before and after giving a very low dose of an adrenaline -like drug (dobutamine). The patient will already have received this short acting drug (at the same and higher doses) during their routine care planning stress echocardiogram. The investigators will also measure the pressure across the aortic valve, known as the trans-aortic gradient, using the pressure wire (PW) and a standard (multipurpose) heart catheter. The investigators will repeat the resting measures (i.e. without pacing or dobutamine) at the end of the procedure to measure the early change in left ventricular contractility and then repeat the echocardiogram immediately and after 3 months to assess the outcome of the TAVI procedure in terms of left ventricular function volume and function

Recruitment information / eligibility

• Status: Completed
• Enrollment: 7
• Est. completion date: March 1, 2024
• Est. primary completion date: March 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Patients presenting symptomatic AS listed for TAVI

2. Native aortic valve disease

3. Ejection fraction </= 40%

4. Mean trans aortic gradient (echo) of <35 mmHg

5. AVA </= 1cm2

6. Able to give written informed consent prior to enrolment in the study

7. No contraindication to study procedures

8. CT scan confirmed severe AS

9. *Able and willing to return to the implanting site for the follow-up visits*

Exclusion Criteria:

1. Unable to provide formal written consent

2. Known pseudo-severe AS prior to TAVI

3. Known allergy to agents required for stress echocardiography

4. Known hypersensitivity or contraindication to aspirin, heparin, clopidogrel, Nitinol, or sensitivity to contrast media, which cannot be adequately premedicated. *

5. Any clinical contraindication to TAVI procedure This pilot study will be restricted to English speaking subjects.

Related Conditions & MeSH terms

• Aortic Valve Stenosis
• Cardiovascular Abnormalities

Intervention

Other:
• Ultrasound
Participants will have a routine ultrasound of the heart (echocardiogram) before the procedure. During this test we will take a few extra measurements, this will not add any significant time to the scan

Procedure:
• Catheters
During the TAVI procedure 3 catheters (tubes) will be inserted into the blood vessels at the top of the participants legs as per normal standard care (there will be no extra skin punctures as part of the study).
• Soft study wire
Participants will have a soft study wire inserted to measure the pressure in the left ventricle. This step is in addition to standard care.

Radiation:
• X-ray
Participants will have chests x-ray when the soft study wire is inserted.

Drug:
• Dobutamine
Participants will be given a low dose infusion of dobutamine, to make the heart pump quicker and more vigorously.. This will last for approximately 5 minutes

Locations

Country	Name	City	State
United Kingdom	The Royal Wolverhampton NHS Trust	Wolverhampton	West Midlands

Sponsors (1)

Lead Sponsor	Collaborator
The Royal Wolverhampton Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in LV ejection fraction at 3 months compared to pre procedural readings.	Change in LV ejection fraction as a percentage	3 months
Primary	Change in LV Volume at 3 months compared to pre procedural readings.	Change in LV Volume measured by BSA, mL/m2	3 months
Primary	Change in global longitudinal strain at 3 months compared to pre procedural readings.	Change in global longitudinal strain measured by percentage	3 months
Primary	Change in fractional shortening by echocardiography at 3 months compared to pre procedural readings.	Change in fractional shortening measured by percentage	3 months
Primary	The change in contractility (dP/dT) with low dose dobutamine stress prior to TAVI, measured by invasive Pressure Wire	The change in contractility (dP/dT) with low dose dobutamine stress prior to TAVI, measured by invasive Pressure Wire	3 months
Primary	The change in aortic trans-valvular gradient with low dose dobutamine stress during TAVI prior to AV treatment.	The change in aortic trans-valvular gradient measured by mmHg	3 months
Primary	The change in contractility (dP/dT) from pre to post procedure at 3 months.	The change in derivative of pressure over time (dP/dT) is measured by the change in pressure per unit time. Measured ventricular pressure provides an indication of the contractility or relaxation of the ventricles of a heart. In this way, the derivative of pressure over time (dP/dt) provides a biphasic signal that can be used to evaluate acute directional changes of contractility	3 months