Outcome of Balloon Pulmonary Valvuloplasty in Patients With Congenital Pulmonary Stenosis in Terms of Reverse Right Ventricular Remodelling and Functional Exercise Capacity

Outcome of Balloon Pulmonary Valvuloplasty in Patients With Congenital Pulmonary Stenosis in Terms of Reverse Right Ventricular Remodeling and Functional Exercise Capacity

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05828524

Enrollment

Registered

2023-04-25

Start date

2021-01-10

Completion date

2024-12-31

Last updated

2023-04-25

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

Conditions

Congenital Heart Disease, Pulmonary Valve Stenoses

Brief summary

A prospective of 30 patients with symptomatic severe congenital valvular pulmonary stenosis who are indicated for percutaneous balloon pulmonary valvuloplasty . the aim is to 1. \- evaluate electrical and mechanical remodeling of RV 6 months following balloon dilation 2. \- evaluate Functional capacity using 6MWT and SaO2 before and 6 months following BPV

Detailed description

Valvular pulmonary stenosis (PS), defined as an obstruction of blood flow at the level of the pulmonary valve, is a form of congenital heart disease, described in 0.6-0.8 out of 1000 live births. The main physiologic effect of valvular pulmonary stenosis (PS) is an increase in Right ventricular pressure proportional to the severity of obstruction. This elevation of RV pressure is accompanied by an increase in muscle mass where hyperplasia of the muscle cells with a concomitant increase in the number of capillaries occurs. In contrast, the adult myocardium responds with hypertrophy of the existing fibers, with no change in the capillary network. Percutaneous balloon pulmonary valvuloplasty (PBPV) is the procedure of choice for uncomplicated severe or symptomatic pulmonary stenosis. the aim is to 1. \- evaluate electrical and mechanical remodeling of RV 6 months following balloon dilation 2. \- evaluate Functional capacity using 6MWT and SaO2 before and 6 months following BPV

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

16 Years to No maximum

Inclusion criteria

* 1-Adult population with an age more than or equal to 16 years of age at time of procedure 2-Severe valvular Pulmonary stenosis defined as a PG max more than or equal to 64 mmHg measured by 2d echo before Procedure

Exclusion criteria

1. Patients with isolated supra-valvular and sub valvular pulmonary stenosis 2. Patients with peripheral pulmonary stenosis. 3. Patients with pulmonary stenosis if part of another congenital heart disease . 4. Patients with organically diseased Tricuspid valve 5. Patients with any significant shunt lesion which result in dilation in RV such as atrial septal defect. 6. Patients with right ventricular dysfunction due to arrhythmogenic right ventricular dysplasia (ARVD) or non compaction

Design outcomes

Primary

Measure	Time frame	Description
reverse Right ventricular remodeling	one year	reverse right ventricular remodeling detected by cardiac MRI and 2D echocardiography after
functional exercise capacity	one year	assessment of functional exercise capacity by performing six minutes walk test

Countries

Egypt

Outcome results