Assistance in the development of study-specific documents is one of the initial tasks we can provide for our customers before the start of the clinical trial.
We provide assistance in the development of:
In most clinical trials with imaging endpoints sonographers need to be trained before they are eligible for recording patient echos. We provide on-site training and on-line training (e.g. videos, web-based training sessions)
Subsequently sonographers have to submit a evaluation echo study, which will be analyzed by our readers to provide real-time feedback.
If study specific requirements are fulfilled (e.g. all required views recorded) and the quality of the recorded echo is sufficient (according to our specified quality criteria) the sonographer receives a certification document.
Our core business is providing high quality echocardiographic image analysis according to the study-specific analysis plan
We also have a a vast experience with stress echocardiography studies (treadmill and/or dobutamine).
Under certain conditions, it might also be required that ad-hoc image analysis needs to be performed by our core lab (e.g. verification of inclusion criteria).
After the reading, an additional control-reading (“overreading”) is done by our most experienced team members.
We provide LV, LA and RV analysis of conventional and novel cardiac echo parameters: