AcT QuICR Trial
One of the first projects on our DCTMS platform, the AcT trial is a Pragmatic Phase III randomized open-label registry-based trial with blinded end-point assessment. The trial seeks to test whether intravenous tenecteplase (an intravenous thrombolytic drug tested and found safe in multiple phase 2 and one phase 3 trial is patients with acute ischemic stroke) can replace intravenous alteplase (the current standard care) in patients who are otherwise eligible to receive the latter in routine care.
ACT-QUICR is a custom designed Electronic Data Capture (EDC) and Randomization Solution with the purpose of facilitating the data collection for the ACT-QUICR trial, while providing the following functions:
- Provides participating trial physicians with the physician script
- Provides patients with relevant patient information
- Allow randomization of subjects based on the presented protocol
- Provide functionality for validating the randomization of subjects
- Enable paper and electronic subject consent acquisition
- Sends out periodic notifications to enrolled sites
- Dashboards, charts and reports
- Secure & Scalable
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