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Meet Trial Accrual Targets with Confidence

BUILD MORE EFFECTIVE CANCER CLINICAL TRIAL PROTOCOLS

Trial Navigator’s Trial Builder module instantly visualizes the effect of criteria adjustments to save time for principal investigators and ensure each trial is ethical, feasible, and attracts a diverse population.

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Design Inclusion Criteria That Are Precise and Inclusive

Principal Investigators spend a lot of time and effort designing trial protocols. But with limited access to data and a large patient population, they risk excluding suitable patients through selection bias.

Trial Navigator’s Trial Builder module takes the guesswork out of this process, empowering Principal Investigators to:

Eliminate Bias

Overcome data limitations that lead to poor diversity, low accrual rates, and biased trial populations that produce results that are less valid and generalizable.

Increase Trial Accrual

Avoid expensive trial failures and help more patients access cutting-edge treatments by identifying eligible participants within feasible distance of the facility.

Accelerate Trial Planning

Streamline your trial protocol design with intuitive visualization tools and empower principal investigators to seamlessly start patient pre-screening.

Trial Protocol Design

  1. Access accurate population assessments
    The Trial Builder module centralizes all population data and allows you to sort patients based on geographic location, sex, gender, and ethnicity.
  2. Test inclusion criteria
    The tool then enables you to dynamically build and test inclusion and exclusion criteria. You can instantly visualize how each adjustment will impact trial feasibility and diversity.
  3. Optimize your criteria
    Users can then move forward using criteria that ensure they will meet accrual and DEI goals with confidence.

Don’t Let Data Limitations Ruin Your Trials

Stop spending hours building inclusion criteria that exclude eligible patients and lead to abandoned trials.

Use Trial Builder to balance specificity with inclusivity – and complete more successful clinical trials.