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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05363696
Other study ID # 450617006
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 1, 2013
Est. completion date August 1, 2019

Study information

Verified date May 2019
Source University of Sao Paulo General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Cardiovascular diseases remain the leading cause of death for the healthcare system and cardiac surgery has an important impact on their resolubility. Healthcare systems in the world have evolved to optimize their clinical records and thus learn from the real world through the interactivity between results, processes, and structure. When the rate of growth of healthcare costs scenario is greater than the one of Gross Domestic Product of countries, there is a considerable challenge to increment the quality of healthcare services and the primordial patient safety, as well as the necessary control and traceability of implantable devices. The association and correlation of patients' demographic and clinically relevant information with the resources required for the care provided for each stratum represent the possibility to adapt, improve and innovate the healthcare programs; This will allow improving the optimization of the therapeutic protocols and the creation of related research areas, aiming to promote more equitable resources allocation, increase access and effectiveness, as well as to ascertain the magnitude of available and used resources and its impact.


Description:

METHODS Extension Cohort study, mandatory, prospective multicenter, in the state of São Paulo and of registry of consecutive cases. Besides the situational diagnostic of the results and comparison between the mean of both registries, there will be the creation of improvement reports for each of the REPLICCAR centers. Next, quality improvement initiatives will be implemented in each center indicated by the reports. Sample - Will be included in a consecutive way all patients that had CABG and heart valve surgery in the participant centers for the defined period; - Data will be collected, independently of surgical volume, severity status, and social condition among others, in sight of the São Paulo state health department; - This way, it will be possible to produce a predictive curve to be used in most clinical case scenarios observed in the state of São Paulo;


Recruitment information / eligibility

Status Completed
Enrollment 9723
Est. completion date August 1, 2019
Est. primary completion date September 1, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Age 18- 90 years old. - CABG or heart valve surgery - Agreement to participate in the study signing informed consent documentation. Exclusion Criteria: - Re-operation - Impossibility to access data variables relevant to the study.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Coronary artery bypass grafting (CABG)
Coronary artery bypass grafting surgery procedure
Heart valve surgery
Heart valve surgery procedure

Locations

Country Name City State
Brazil Fabio B Jatene, MD, PhD São Paulo
Brazil USP Heart Institute São Paulo

Sponsors (14)

Lead Sponsor Collaborator
University of Sao Paulo General Hospital Beneficência Portuguesa de São Paulo, Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto - USP, Hospital das Clinicas da Universidade Estadual de Campinas, Hospital de Base de São Jose do Rio Preto, Hospital Israelita Albert Einstein, Hospital Pitangueiras do Grupo SOBAM, Hospital Samaritano Paulista, Hospital São Paulo da Universidade Federal de São Paulo, Instituto Dante Pazzanese de Cardiologia, Instituto do Coração do Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, Irmandade da Santa Casa de Misericórdia de Marília, Irmandade da Santa Casa de Misericórdia de Piracicaba, Irmandade da Santa Casa de Misericórdia de São Paulo

Country where clinical trial is conducted

Brazil, 

References & Publications (1)

Orlandi BMM, Mejia OAV, Borgomoni GB, Goncharov M, Rocha KN, Bassolli L, Melo de Barros E Silva PG, Nakazone MA, Sousa A, Campagnucci VP, de Sousa Vilarinho KA, Katz M, Tiveron MG, Arrais Dos Santos M, Lisboa LAF, Dallan LAO, Jatene FB; REPLICCAR II Study — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Create and implementing data driven quality initiatives for cardiac surgery procedures in São Paulo state Guided by the database, quality initiatives will be built in order to reduce mortality, length of stay and complications in the centers participating in REPLICCAR. 5 years
Secondary Create a morbidity and mortality risk score Create a morbidity and mortality risk score, in order to guide the care and interventions of patients undergoing cardiac procedures, in order to prevent morbidity and mortality outcomes. 5 years
Secondary Long-term follow-up of patients included in the database Long-term follow-up of patients included in the database, providing an opportunity to assess quality of life, evolution and deaths after hospital discharge. 10 years
Secondary Assessment of the impact of patients' socioeconomic variation in its surgical evolution Assessment of the impact of patients' socioeconomic variation on their evolution in terms of morbidity and mortality (short and long term). 10 years
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