What does CCRF mean in CLINICAL MEDICINE

The Cardiovascular Clinical Research Facility is a specialized research center that conducts clinical trials for cardiovascular related diseases. It provides state-of-the-art medical equipment and personnel to assess patient health outcomes. The facility offers comprehensive research infrastructure and resources enabling investigators to conduct clinical trials of cardiovascular drugs, devices, therapies and other interventions.

People suffering from any type of heart disease, including ischemic heart disease or atherosclerosis, can benefit from the CCFR services through participating in clinical trials. Additionally, people interested in furthering their understanding of cardiovascular care may take advantage of educational opportunities provided by the facility.

Tests available at the CCFR include echocardiograms, stress tests, electrocardiograms (ECGs), vascular ultrasound scans, and cardiac catheterization procedures amongst others. The CCFR also offers laboratory testing to measure metabolic parameters such as cholesterol levels, blood pressure readings and other biomarkers associated with heart health.

To find out about upcoming clinical trials at the CCFR you can visit their website to review all current research studies that are open for enrollment. You can also sign up for email notifications about new or upcoming studies so that you can stay informed about opportunities to participate in groundbreaking research initiatives being conducted at this facility.

Clinical trial lengths vary based on individual study protocols; however most trials typically last between one–two years or more depending on complexity of study requirements.

The safety regulations of each trial conducted at CCRF are overseen by an Institutional Review Board (IRB) which is comprised of an independent group including physicians, statisticians and ethicists who review study protocols prior to initiation then monitor safety during each participant’s involvement in a trial phase.

Yes! All participant records will be kept confidential and secure and will only be accessible by approved personnel conducting a study at CCRF. Participants will have full access to their own medical records throughout their participation in a trial.

Depending on the nature of the study some participants may receive compensation for time or expenses incurred while taking part in a clinical trial. Payments for participation vary depending on complexity or duration but all payments must be approved by investigators prior to disclosure.

Each trial has different eligibility criteria that must be followedfor participants; however generally speaking individuals must meet predetermined age requirement as well as have no previous history with any investigated condition within 2 years prior enrolment date.