Acute and chronic analgesic clinical trials

The only platform built specifically for analgesic trials that trains your entire site, clinical and non-clinical, not just who is on the delegation log.

Placebo response is shaped by everyone who interacts with a subject. TrialTron trains all of them, at a level appropriate to their role.

< 15 min
Escalation SLA
NRS-A · NRS-R · PGA · PGIC · VRS
Validated scales
10 roles
Trained per site
21 CFR Part 11
Compliant

A clean signal. A site you can trust to know what to do.

Standard Site Training
TrialTron
Trains what gets audited
Trains what actually shapes the signal
Front desk, schedulers, and recruiters trained informally, if at all
Every role trained, calibrated to what that role actually does
Scale administration varies rater to rater
Standardized scale administration, every rater, every visit
Placebo response is modeled by a biostatistician after unblinding
Placebo response is controlled for before first subject in
Placebo response gets attributed to the disease, not the site
A site the sponsor can trust to get it right, visit after visit

Why neutral, transactional language is the mechanism

“How are you feeling today?” is not a neutral question. It is an expectation-setting event, delivered before the subject ever picks up an NRS.

TrialTron replaces well-intentioned warmth with tested, transactional phrasing at every touchpoint, so a subject’s reported pain reflects the drug, not the conversation around it.

What we train

Every module scoped to the role and grounded in the specific behaviors that inflate placebo response.

Site Staff
Scale administration

NRS-A, NRS-R, VRS, PGA, and PGIC delivered the same way by every rater, removing examiner drift.

Neutral, transactional language

Tested phrasing for every subject touchpoint, so tone never becomes a variable in the data.

Expectation management

Front desk and scheduling staff trained on how tone and framing shift reported pain.

Rescue medication documentation

Staff trained on precise timing and reason capture, replacing vague entries like "subject request" with what the protocol actually requires.

Protocol-driven escalation

Trained to catch and escalate what the protocol requires — eligibility flags, required captures, anything material — not just adverse events.

Subject
How to use the scale

Subjects calibrated on NRS and VRS before first assessment — what the anchors mean, how to use the full range, and why consistency across visits matters.

What to expect during the study

Structured orientation covers visit flow, timing of assessments, and what constitutes a reportable event, without language that sets treatment expectations.

Accurate symptom reporting

Subjects trained to report pain as it is right now, not averaged, not influenced by the last visit — reducing recall bias and visit-to-visit drift.

Rescue medication rules

When rescue is allowed, how to request it, and why precise timing matters — so subject-reported rescue use matches the protocol record.

Study communication boundaries

Subjects understand what questions staff can and cannot answer, reducing the pressure on coordinators to say things they should not.

Why TrialTron exists

TrialTron was founded by a board certified anesthesiologist and principal investigator with deep, hands-on clinical research experience. Her focus is acute and chronic pain trials, inpatient and outpatient. Her sites are known for clean data.

What she saw was a gap no software had addressed: a standardized way to train site staff on why their tasks matter to the endpoint, and to educate subjects on how to report pain in a way that holds up across visits, raters, and sites. That standardization is what turns a subjective endpoint into defensible data — the kind sponsors can stand behind at submission. TrialTron is built to deliver it, from the protocol level, not from a software requirements document.

Ready to run a cleaner analgesic trial?

Pilot deployment in 48 hours. Schedule a walk-through with a team member who has run a pain study.

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