- Ambulatory Standard 12-Lead ECG machine
- 24h to 7 days Holter ECG Monitoring
- Blood Pressure Monitoring
- Continuos ECG Monitoring
- Continuous SpO2 Monitoring
- ECG Telemetry
- MasterLab (Jaeger), Oxycon Pro (Jaeger) and Dosimeter (Jaeger) for Lung function evaluation
- Galileo System Sirius for EEG
- Lion alcolmeter S-D2 for Alcohol breath test
- Micro smokerlyser CO for CO monitoring
In collaboration with the CRC it is possible to have access to the hospital instrumentation too.
Special subject populations (i.e. elderly, post-menopausal, impaired liver function, paediatric) can be recruited as well as defined disease groups (i.e. cardiovascular, respiratory, neurological, pancreatic, gastrointestinal, urological, metabolic and psychiatric) for Proof-of-Concept studies.
The CRC database consists of approximately 650 active male and female healthy volunteers, with a good level of education, that enables a better comprehension of our documents and activity. The majority of volunteers are a word-to-mouth source, as volunteers talk with friend about their experience of taking part in a clinical trial. The application process is designed to ensure that a volunteer is a suitable candidate for clinical studies.
The first stage in the screening process is a Health Questionnaire to be filled in by the potential volunteer. The Questionnaire is accompanied by an Information Sheet and a Declaration of Consent: both documents must be signed and dated by the volunteer.
After the Unit Doctor’s evaluation of the application form, the suitable subject is invited to our centre to carry out some more tests in order to gain more information about him/her (i.e. Fagerström Questionnaire about smoking habits, STAI-Y test for anxiety level) and the MMPI-2 test (Minnesota Multiphasic Personality Inventory) for people under 64 years old or Zung’s self-rating depression and anxiety scales for people older than 64. These personality tests are evaluated by a Psychologist and become an inclusion/exclusion criteria.
Joining the Panel does not oblige a volunteer to take part in a clinical study. The volunteer is able to withdraw from the Panel at any time. The volunteer will be asked to take part in a screening medical only during a study-specific screening.
A PANEL with about 650 subjects has been set up.