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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05523193
Other study ID # 2022-07
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date August 1, 2022
Est. completion date August 31, 2024

Study information

Verified date August 2022
Source Second Affiliated Hospital of Nanchang University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Study Title: A real-world study of valvular heart disease in Jiangxi Province Research Objectives: ① Main objectives: To examine the current incidence of valvular heart disease in Jiangxi Province, to establish a "Formal treatment model" for patients with valvular heart disease, and to manage the collection of diagnostic, therapeutic and prognostic data on patients. ② Secondary objective: To investigate the composite of all-cause mortality, disabling stroke, permanent pacemaker implantation, and moderate or greater valve regurgitation in the "Formal treatment model" group and the "Conventional treatment model" group. The Conventional group was matched to patients who were not in the " Formal treatment model " during the same period. Design type: a prospective, observational, real-world study (at least 1.5 years). No pre-established fixed treatment protocols, only a Formal treatment model,with all treatment choices made entirely by clinicians following relevant textbooks, expert consensus on clinical guidelines, and based on the patient's condition. Subjects: All patients with moderate to severe heart valve disease were collected from the Second Affiliated Hospital of Nanchang University and hospitals at all levels in Jiangxi Province from September 2022 to September 2023.


Description:

Summary of Research Protocol: Study Title: A Real World Study of Valvular Heart Disease in Jiangxi Province Research Objectives: ① Main objectives: To examine the current incidence of valvular heart disease in Jiangxi Province, to establish a "Formal treatment model" for patients with valvular heart disease, and to manage the collection of diagnostic, therapeutic and prognostic data on patients. ② Secondary objective: To investigate the composite of all-cause mortality, disabling stroke, permanent pacemaker implantation, and moderate or greater valve regurgitation in the "Formal treatment model" group and the "Conventional treatment model" group. The Conventional group was matched to patients who were not in the " Formal treatment model " during the same period. Design type: a prospective, observational, real-world study (at least 1.5 years). No pre-established fixed treatment protocols, only a Formal treatment model,with all treatment choices made entirely by clinicians following relevant textbooks, expert consensus on clinical guidelines, and based on the patient's condition. Subjects: All patients with moderate to severe heart valve disease were collected from the Second Affiliated Hospital of Nanchang University and hospitals at all levels in Jiangxi Province from September 2022 to September 2023. Formal treatment model group: Patients who agree and accept the surgical treatment recommendation (including medical and surgical treatment) enter the formal treatment model group. Those who have received any of the following treatments (including but not limited to) as recommended by the standardized treatment process are considered to have received the standardized treatment, otherwise, they have not. 1. Surgical procedures: valve repair or replacement, left auricular ligation, left auricular clip. 2. Internal surgery: transcatheter valve replacement, radiofrequency ablation of atrial fibrillation, and left heart ear occlusion. Conventional treatment model group: Patients who do not agree to enter the Formal treatment model group will automatically enter the Conventional treatment model group.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1052
Est. completion date August 31, 2024
Est. primary completion date August 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All moderate-to-severe heart valve disease, including aortic, mitral, and tricuspid valves; - Comply with the ESC/EACTS Guidelines for the Management of Valvular Heart Disease (2021) indications for surgery for valvular heart disease; - Understand and voluntarily sign the informed consent form Exclusion Criteria: - those with severe mental disorders and unable to express their will; - those with obvious other abnormal signs, laboratory tests and clinical diseases that, in the judgment of the investigator, make them unsuitable for participation in the study; - those who, in the judgment of the investigator, are unable to complete long-term follow-up.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Formal treatment model
Formal treatment model , no further surgery or minimally invasive treatment was performed

Locations

Country Name City State
China The Second Affiliated Hospital of Nanchang University Nanchang Jiangxi

Sponsors (1)

Lead Sponsor Collaborator
Xiao Huang

Country where clinical trial is conducted

China, 

References & Publications (5)

Carità P, Coppola G, Novo G, Caccamo G, Guglielmo M, Balasus F, Novo S, Castrovinci S, Moscarelli M, Fattouch K, Corrado E. Aortic stenosis: insights on pathogenesis and clinical implications. J Geriatr Cardiol. 2016 Sep;13(6):489-98. doi: 10.11909/j.issn — View Citation

Cary T, Pearce J. Aortic stenosis: pathophysiology, diagnosis, and medical management of nonsurgical patients. Crit Care Nurse. 2013 Apr;33(2):58-72. doi: 10.4037/ccn2013820. Review. — View Citation

Dweck MR, Boon NA, Newby DE. Calcific aortic stenosis: a disease of the valve and the myocardium. J Am Coll Cardiol. 2012 Nov 6;60(19):1854-63. doi: 10.1016/j.jacc.2012.02.093. Epub 2012 Oct 10. Review. — View Citation

Sathyamurthy I, Alex S. Calcific aortic valve disease: is it another face of atherosclerosis? Indian Heart J. 2015 Sep-Oct;67(5):503-6. doi: 10.1016/j.ihj.2015.07.033. Epub 2015 Aug 21. Review. — View Citation

Soler-Soler J, Galve E. Worldwide perspective of valve disease. Heart. 2000 Jun;83(6):721-5. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Primary endpoints all-cause mortality, disabling stroke, and incidence of cardiogenic stroke, permanent pacemaker implantation rate, and moderate or greater valve regurgitation at 1 year after surgery or discharge from treatment 1 year after surgery or treatment
Secondary All-cause mortality Including cardiac death and non-cardiac death surgery or 30 days after treatment
Secondary incidence of stroke The incidence of stroke 30 days after discharge from hospital after surgery or treatment 30 days after discharge from hospital after surgery or treatment
Secondary rate of permanent pacemaker implantation The rate of permanent pacemaker implantation after surgery or 30 days after treatment surgery or 30 days after treatment
Secondary Moderate or higher valvular regurgitation Moderate or higher valvular regurgitation after surgery or 30 days after discharge immediately after the surgery or 30 days after discharge
Secondary Readmission rates for aortic stenosis and/or valve implantation-related complications Readmission rates for aortic stenosis and/or valve implantation-related complications at 30 days and 1 year after surgery or treatment 30 days and 1 year after surgery or treatment
Secondary The incidence of intraoperative temporary valve size replacement including increasing or decreasing valve size intraoperative
Secondary The incidence of abnormal valve position including valve displacement, valve embolism, and valve ectopic release during operation
Secondary The incidence of implantation of two or more valves The incidence of implantation of two or more valves during aortic valve replacement during aortic valve replacement
Secondary The Barthel index The Barthel index was used to evaluate the health status of the subjects 30 days and 1 year after surgery or treatment
Secondary NYHA classification NYHA classification at 30 days and 1 year after discharge after surgery or treatment 30 days and 1 year after discharge after surgery or treatment
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