Actively Recruiting
Results of the Aortic Valve Reconstruction in Children
Led by National Medical Research Center for Children's Health, Russian Federation · Updated on 2021-03-03
40
Participants Needed
1
Research Sites
397 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Aortic valve disease counts up to 5% of cases of congenital heart disease being one of the most common congenital malformations of the cardiovascular system. This disease requires replacement of the damaged valve which in itself is not a trivial task to complete in children as there is still no available best practice for valve replacement. Today, the following alternative variants are performed in children: mechanical aortic prosthesis, xenografts, allografts, and pulmonary autograft (Ross procedure) and each has its potential advantages and disadvantages. Mechanical aortic prostheses require lifelong anticoagulation therapy and repeated surgeries to replace mechanical valves during child growth. Available xenografts in children also has suboptimal results not only because of absence of growth potential, but also due to development of degenerative changes in biological tissue of the graft leaflets. Allograft tissues are exposed to rapid biodegradation in the recipient body and thus requiring repeated surgeries associated with higher difficulty, high risk of hemorrhages, and injury of the coronary injuries. Ross procedure was proposed as theoretically the most evidence-based reconstruction of the aortic valve in children. Even successfully performed Ross operation transforms one-valve disorder into two-valve disease. The accumulation of knowledge on the anatomy of the aortic root and improvement of surgical techniques led to the development of new methods for reconstruction of the valve function. The technique is widely applied in adult cardiac surgery, uses glutaraldehyde-treated autopericardium for augmentation of the leaflets. Absence of foreign material provides no need for anticoagulation therapy. Potentially, reconstruction of the aortic valve with autopericardium can be widely used in children. Aim is to study safety, clinical and hemodynamic efficacy of the method of the aortic valve reconstruction with autopericardium in children with aortic valve disease. Patients aged 29 days to 12 years will be included into the study. The data according to the protocol of the study will be assessed at the stage of inclusion, during the surgery, in 30 days after the surgery, and in 1, 2, and 3 years after the surgery. Data about all the patients included into the research will be analyzed in order to study the endpoints and achieve the research aim.
CONDITIONS
Official Title
Results of the Aortic Valve Reconstruction in Children
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age from 29 days to 12 years
- Official caregivers must provide informed consent after study explanation
- Patients with aortic valve issues including mean gradient over 40 mmHg with normal heart function, or severe aortic insufficiency, or other specific valve dysfunctions
- Aortic Z-score over -1.5
- No subvalvular or supravalvular aortic stenosis
- No intracardiac malformations needing correction, except septal defects
You will not qualify if you...
- Known allergies to aspirin, heparin, nitinol, or intravenous contrast, or contraindications to these
- Previous aortic valve replacement with mechanical or xenografts
- Active infection such as sepsis or endocarditis
- Hypoplasia of the aortic valve fibrous ring with Z-score under -1.5
- Life expectancy less than 3 years due to other diseases
- Participation in other clinical research
- Urgent need for surgery
- Intracardiac malformations requiring immediate surgery
- Unstable living situation complicating study follow-up
- Caregivers refuse continued participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Medical Research Center of Children's Health
Moscow, Russia, 119296
Actively Recruiting
Research Team
V
Vladimir P. Miroshnichenko, PhD
CONTACT
A
Alexander A. Lezhnev, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here