Diamind

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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