Run Clinical Trials on Data
Already Being Collected.
Subjects using N1 Precision Insights log seizures, medications, and daily events every day. Trials transforms that real-world data into a structured clinical research platform.
No new burden on subjects. No transcription errors. Cohort management, multi-site coordination, and audit-ready reporting — all built in.
How It Works
From Patient Logging to Trial Data
The data collection infrastructure already exists. Trials connects it to clinical research workflows with cohort management and audit-ready reporting.
Enroll Subjects
Subjects already using N1 Precision Insights are enrolled into your trial. No new apps, no new workflows — data collection is already happening.
Data Flows Automatically
Seizure logs, medication changes, and daily assessments flow from Insights into the Trials platform in real time — structured and timestamped.
Manage Cohorts
Organize subjects by site, arm, or custom criteria. Track enrollment, retention, and protocol adherence across your entire study.
Analyze & Report
Run multivariate analysis, linear regression, and cluster detection across your cohort. Export audit-ready reports for regulatory documentation.
Advanced Reporting
Advanced Analytics for Trial Teams
Purpose-built analytical tools for clinical research. Run cohort-level analyses across your entire study population. Observational data exploration — not clinical decision support.
Multivariate Analysis
Examine how medications, sleep, diet, and daily events interact to influence seizure patterns — beyond what single-variable views can show.
Linear Regression
Model seizure frequency trends over time against medication changes, dosage adjustments, and environmental factors.
Seizure Cluster Analysis
Detect temporal clustering patterns, identify triggers that precede clusters, and measure inter-cluster intervals across the full history.
AI-Powered Data Exploration
The patient's complete longitudinal record — every seizure, medication, lab result, and daily event — loaded into an AI for natural-language exploration and data summarization. All outputs are observational — not clinical decision support.
Platform Capabilities
Built for Rigor. Designed for Reality.
Every feature exists to bridge the gap between real-world patient data and clinical trial standards.
Automated Data Collection
Seizure logs, medication changes, and daily assessments captured at the source — by the people who know the patient best.
Data Quality Scoring
Every record is scored for completeness and consistency. Missing data is flagged before it becomes a problem.
Cohort Management
Organize subjects by site, arm, or custom criteria. Track enrollment, retention, and protocol adherence at a glance.
Statistical Reporting
Pre-built and custom reports for seizure frequency, medication response, and quality-of-life outcomes across your cohort.
IRB-Ready Data Architecture
HIPAA-eligible infrastructure, BAA available, and IRB-ready data architecture. Immutable data provenance, timestamped records, and exportable audit trails.
Multi-Site Coordination
Unified dashboards across sites. Standardized data collection ensures consistency regardless of location.
Interested?
Run Your Next Epilepsy Trial on Real-World Data
N1 Precision Trials is in active development. If you're a principal investigator, research coordinator, or institution planning an epilepsy trial, we'd love to discuss how existing patient data can power your study.
Contact UsN1 Precision Trials is designed for research compliance. HIPAA-eligible infrastructure, BAA available, IRB-ready data architecture. It is not a medical device, clinical decision support system, or FDA-regulated software. All outputs are observational summaries of logged data.