Cardiology clinical trials

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Cardiology clinical trials

These trials often involve patients with multiple comorbidities who are often elderly. As cardiovascular diseases affect various populations differently, it is key to include a diverse population in your clinical trial.
Moreover, in some indications such as stroke, patients may require support from caregivers, whose perspective must also be considered.
With specific patient profiles, inclusion and exclusion criteria can be particularly strict, and study procedures can also be complex. This creates a challenging operational environment.

“In cardiology clinical trials, the use of eCOA has been transformative. It allows for real-time data collection and patient monitoring, which is crucial given the complex comorbidities and elevated age of many participants. This technology not only enhances data accuracy but also ensures diverse patient representation, leading to more comprehensive and reliable results.“

Estelle Haenel, Kayentis Chief Medical Officer

At Kayentis, we have the experience of such complex studies. Our expert project teams, our robust data management systems, and our strong and intuitive eCOA solution combine to ensure the success of your trial.

Streamline your cardiology clinical trial with our expert eCOA guidance

Leveraging our extensive experience in cardiology trials, we provide comprehensive support from the moment you start to design your study.

Work with our scientific and clinical experts to establish your project endpoints, choose the most appropriate PRO measures, develop an effective eCOA strategy, and enhance the experience for patients, caregivers, and sites.
Rely on our skilled teams and meticulous processes to manage the complexities of your clinical trials, including quick study set up, multiple management roles, and robust processes for managing long studies, large volumes of data, and frequent amendments.
Introduce strong engagement features to ensure comfort and minimize the burden on patients, caregivers, and site staff.

Easily capture crucial trial data with our intuitive eCOA solution for your cardiology studies

eConsent: Depending on patient health status and patient profile we optimize the management of on-site or remote consent, as well as re-consent processes.
Flexible data collection: Benefit from a variety of data collection methods, including ergonomic provisioned devices or BYOD, to ensure comfort for patients, caregivers, and clinicians.
Instant reporting: Clinicians can quickly access our Clin’form WebPortal for real-time monitoring of clinical data and patient compliance.
Audit trail and traceability: Attributability of the data is always possible thanks to solid audit trail capabilities, which is even more important in situations where patients are disabled and not able to complete their questionnaires themselves.