Oncology trials live or die on safety data quality and dosing accuracy. Capture gives you AE and SAE forms, BSA-based dose calculations, and randomization for blinded arms, all in one audit trail, so a small oncology team can run the same rigor as a large one.
Free sandbox · No credit card · 21 CFR Part 11 aligned
BMI (Body Mass Index)
Auto-derivedHeight (cm)
172
Weight (kg)
68.5
Result
23.2 kg/m²
Reference: WHO · shown read-only during data entry
2
BSA formulas built in: Mosteller and Du Bois
Field-level
audit trail on every safety record
Auto
query raised the moment a lab value breaks a rule
Free
sandbox with sample data
Dosing accuracy
Oncology dosing frequently depends on body surface area. Turn any field into a calculated one, map it to the height and weight questions already on the form, and the value fills itself in automatically, so a transcription error cannot change what a patient is dosed.
BMI (Body Mass Index)
Auto-derivedHeight (cm)
172
Weight (kg)
68.5
Result
23.2 kg/m²
Reference: WHO · shown read-only during data entry
Safety reporting
Pre-built templates for adverse events, serious adverse events and adverse events of special interest sit alongside your other case report forms, sharing the same audit trail. A safety signal is visible the moment a site enters it, not weeks later at a data lock.
Cannot submit yet
Causality is required because the event is serious.
Blinded arms
Many oncology designs randomize to arm or dose cohort while keeping site staff blinded. Capture’s randomization module supports blinded views by role, so a site coordinator sees what they need without seeing the allocation.
Study status Live
Site activated Yes
Randomization list 42 allocations left
Has the subject signed the current informed consent?
Before you switch
Every plan, including the free sandbox, includes edit checks, calculated fields and the audit trail.
21 CFR Part 11-aligned controls throughout; documentation available on Enterprise to support your own validation.
AI drafts your visit schedule and forms from a protocol; most teams have a working build the same day.
Bring an existing study or a prior protocol’s forms across as a starting template.
Email support, typically under 24 hours, plus documentation for your own assessment on Enterprise.
Free sandbox with every feature. No credit card, no sales call.
Yes. Build a study arm or cohort structure in the study builder and use randomization to allocate patients within it, with role-based views that keep the blind where your design requires it.
Yes. BSA (Mosteller and Du Bois), along with BMI and other derived values, can be set up as a calculated field that fills in automatically and read-only from the height and weight already entered.
Yes. Adverse event, serious adverse event, adverse event of special interest and concomitant medication templates are in the template library, alongside demographics, vitals and lab forms.
Yes. Export by site or date range with an automatic data dictionary, so your safety or biostatistics team can prepare a review without manually assembling data from separate files.
Yes. The built-in edit checks and auto-queries catch out-of-range values as they are entered, which reduces how much a small team needs to review manually after the fact.
Nothing to start. The free sandbox has no credit card and no time limit. You pay only once you go live with real participant data.
Keep exploring
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Clinical trial randomization software
More on blinded and unblinded allocation.
Audit-ready clinical trial data
The field-level audit trail behind every safety record.
EDC for cardiology clinical trials
The same platform, a different therapeutic area.
CRF builder for clinical trials
How the AI drafts forms and lab tables.
Free sandbox with every feature. No credit card, no sales call.