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Left Ventricular Reverse Remodeling In Aortic Valve Replacement With Single Strip Pericardium Versus Mechanical Valve

Left Ventricular Reverse Remodeling in Aortic Valve Replacement With Single Strip Pericardium and Mechanical Valve: A Comparative Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04056832
Enrollment
62
Registered
2019-08-14
Start date
2017-04-20
Completion date
2020-04-20
Last updated
2019-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Stenosis, Aortic Valve Calcification, Aortic Valve Stenosis, Valve Stenoses, Aortic

Keywords

Aortic Stenosis, Aortic Valve Replacement, Single Strip Pericardium, Autologous Pericardium, Mechanical Valve Replacement, Comparison of Left Ventricle Remodeling

Brief summary

Aortic stenosis is a commonly found heart disease, which often leads to mortality and morbidity. Valve replacement using mechanical prosthetic valve will have an expensive cost especially in the Integrated Heart Center of Cipto Mangunkusumo Hospital, Jakarta, Indonesia. In addition to the expensive cost, patients who have mechanical prosthetic valve have an increased risk of infection of the prosthetic valve and developing thrombo-embolism thus have to consume a lifelong anticoagulant therapy that increase risk of bleeding. A surgical technique using autologous pericardium is an alternative to prosthetic valve replacement, one of which is a single pericardium strip technique that uses modified autologous pericardium technique from Ozaki et al and Duran et al. The objective of this study is to investigate the outcome of aortic valve replacement with a single pericardium strip of autologous pericardium in patients with aortic stenosis. This study will be conducted at the Integrated Heart Center of Cipto Mangunkusumo Hospital, Jakarta, Indonesia, by using quasi experimental type time series design. Subjects are patients with aortic stenosis who are candidates for valve replacement. Inclusion criteria is having low to moderate surgical risk (EuroScore II \<5). The sampling method used in this study is non-probability consecutive sampling. This study will assess the outcome of the aortic valve replacement (valve hemodynamic, left ventricular reverse remodelling, sST2, 6MWT) at 3 months and 6 months post-aortic valve replacement. It is expected that aortic valve replacement using a single strip of autologous pericardium will have good valve hemodynamic outcome, yield left ventricular reverse remodelling, decrease sST2 level, show upgrade in 6MWT, and have shorter aortic cross clamp time so that it can be an alternative to aortic valve replacement using mechanical prosthetic valve that is less expensive and have good outcomes in patient with aortic stenosis.

Interventions

PROCEDURESingle Strip Pericardium

The anterior pericardium is taken in accordance with the measurements made using an aortic annulus sizer or Ismail sizer. The diameter of the annulus valve is converted to circumference of the aortic valve according as a measure of the length of the pericardium. Measurement of aortic commissure height is done by measuring the distance between the lowest point of the valve attachment to the highest point on the commissure as a measure of pericardium width. The pericardium is immersed in 0.6% glutaraldehyde solution for 10 minutes, then rinsed and soaked with saline solution 3 times for 6 minutes each. After the pericardium becomes firm it is cut to be a single strip according to the length and width in the previous measurement. It is then sutured to the aortic valve annulus.

PROCEDUREMechanical Prosthetic Valve

Median incision is performed at the surgical site. Sternal retractor is placed at the sternum after median sternotomy being performed. Aortic valve is measured using aortic annulus sizer. Pledgeted suture is performed for the mattress. Sutures are performed to attach the mechanical prosthetic to the aortic annulus.

Sponsors

Fakultas Kedokteran Universitas Indonesia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged more than 10 years old * Patients with aortic valve stenosis with an indication of aortic valve replacement having low to moderate surgical risk (EuroScore II \<5) * The patient or guardian (the research subject's parent) agrees to follow the study

Exclusion criteria

* Patients who have previously underwent aortic valve replacement * Patients with aortic stenosis due to bicuspid aortic valve * Patients with autoimmune disease * Patients with mixed connective tissue disease

Design outcomes

Primary

MeasureTime frameDescription
Change in 6 Minute Walking Test Performance (METs)before surgery, 3 months and 6 months after surgeryThe result of distance in meters of the six minute walking test will be converted to VO2max by the given formula: (distance in meters x 0.03) + 3.98 = VO2max Then the VO2max will be converted to METs by given formula: VO2max : 3.5 = METs
Change in Soluble Suppression of Tumorigenicity-2 (sST2) Levelbefore surgery, 3 months and 6 months after surgeryLevel of soluble Suppression of Tumorigenicity-2 measured in nano gram per mili Liters (ng/mL) by quantitative sandwich enzyme immunoassay technique assessed with Quantikinine Elisa
Change in Left Ventricular End Diastolic Diameterbefore surgery, 3 months and 6 months after surgeryLeft Ventricular End Diastolic Diameter in mili meters assessed by Trans-thoracic Echocardiography measurement on M-mode
Change in Left Ventricular End Systolic Diameterbefore surgery, 3 months and 6 months after surgeryLeft Ventricular End Systolic Diameter in mili meters assessed by Trans-thoracic Echocardiography measurement on M-mode
Change in Ejection Fraction Percentagebefore surgery, 3 months and 6 months after surgeryEjection Fraction Percentage assessed by Trans-thoracic Echocardiography with modified Simpson's volumetric method (BiPlane measurement: apical 4 chambers and apical 2 chambers)
Change in 6 Minute Walking Test Performance (meters)before surgery, 3 months and 6 months after surgerySubjects will be asked to walk for six minutes on a given track then the distance achieved will be measured in meters

Secondary

MeasureTime frameDescription
Aortic Jet Velocity Value in m/sbefore surgeryAortic Jet Velocity value measured in meters per second (m/s) by Color Wave Doppler on Trans-thoracic Echocardiography
Mean Trans-aortic Pressure Gradient Value in mmHgbefore surgeryMean Trans-aortic Pressure Gradient Value measured in mili meters Hydrargyrum (mmHg) with Bernoulli equation on Trans-thoracic Echocardiography
Aortic Regurgitation Severitybefore surgeryAortic Regurgitation Severity classified as mild, moderate, and severe based on Recommendations from American Society of Echocardiography
Number of Valve Replacement and/or Repairat the time of surgeryNumber of valves being replaced and/or repaired
Aortic Cross Clamp Time in minuteat the time of surgeryThe time from Aortic Cross Clamp On to Cross Clamp Off
Aortic Stenosis Severitybefore surgeryAortic Stenosis Severity classified as mild, moderate, and severe based on Recommendations from European Association of Echocardiography and American Society of Echocardiography (EAE/ASE)
Surgery Time in minuteat the time of surgeryThe time from first incision to finished closing surgical wound
Cardiopulmonary Bypass Time in minuteat the time of surgeryThe time from begin Cardiopulmonary Bypass (CPB) On to CPB Off
Duration of Hospitalizationat the time of surgeryNumber of days of Hospitalization since admission date to discharge date
Coaptation Height of Aortic Valve Leaflet in mili metersat the time of surgeryAortic Valve Coaptation height measured in mili meters by Trans-oesophageal Echocardiography on mid-oesophageal long axis view
Effective Height of Aortic Valve in mili metersat the time of surgeryEffective Height of Aortic Valve measured in mili meters from Aortic annulus to the highest point of Aortic Valve coaptation by Trans-oesophageal Echocardiography in mid-oesophageal long axis view

Other

MeasureTime frameDescription
Duration of Intensive Care Unit Stayat the time of surgeryNumber of hours in the Intensive Care Unit since after the surgery until subject is transferred to hospital ward
Duration of Ventilator Useat the time of surgeryNumber of hours of breathing assisted with ventilator since intubation until extubation

Countries

Indonesia

Contacts

Primary ContactIsmail Dilawar, doctor
ismail_dilawar@yahoo.com+6281310567075
Backup ContactNusaibah N Juliafina, doctor
nusaibahjuliafina@gmail.com+6281210189732

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026