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Coming Soon - Currently in Clinical Trials

METRION Phantom: Revolutionary In-Vivo Calibration

Transform ADC measurements from qualitative patterns to quantitative biomarkers with our groundbreaking embedded phantom technology

METRION System Components

  • Temperature-stabilized embedded phantom
  • Real-time calibration software
  • NIST-traceable reference standards
  • Automated PACS integration

The Challenge: ADC Variability in Prostate Cancer Diagnosis

Current Limitations

  • ADC values vary up to 45% between scanners
  • No standardised reference during patient scans
  • Temperature variations affect measurements
  • Limited ability to track disease progression

Clinical Impact

  • 33% of patients receive unnecessary biopsies
  • Inconsistent results across imaging centers
  • Difficulty in multi-site clinical trials
  • Reduced confidence in quantitative biomarkers

The METRION Solution: Real-Time In-Vivo Calibration

METRION represents a paradigm shift in quantitative MRI. By embedding calibration directly into the patient scan, we transform ADC measurements from relative patterns to absolute, traceable values.

45% → 4.3%

Reduction in ADC measurement variability

Real-Time

Calibration during every patient scan

NIST Traceable

Absolute measurements with known uncertainty

How METRION Works

1

Patient Positioning

The METRION phantom replaces a standard couch cushion. Patients lie naturally on the temperature-stabilized phantom containing NIST-traceable reference markers.

2

Simultaneous Acquisition

Reference markers appear in the same field of view as the patient anatomy. The embedded thermometry system continuously monitors and records temperature.

3

Automated Calibration

The METRION software automatically identifies reference markers, applies temperature corrections, and generates a calibration transfer function specific to that scan.

4

Corrected ADC Maps

Calibrated ADC maps with confidence intervals are automatically generated and sent to PACS, providing radiologists with traceable, quantitative measurements.

Technical Specifications

Embedded Phantom

  • Dimensions: 500mm × 400mm × 60mm
  • Weight: < 5kg
  • Reference Vials: 8 temperature-stable markers
  • ADC Range: 0.3 - 2.5 × 10⁻³ mm²/s
  • Temperature Stability: ±0.5°C via phase-change materials
  • Thermometry: 4-channel fiber optic system
  • Battery Life: > 12 hours continuous monitoring
  • MR Safety: 1.5T and 3T conditional

Calibration Software

  • Integration: DICOM-compatible PACS integration
  • Processing Time: < 2 minutes per study
  • Marker Detection: AI-powered automatic segmentation
  • Calibration Model: Multi-point linear/polynomial fitting
  • Uncertainty Quantification: 95% confidence intervals
  • Temperature Correction: Real-time adjustment algorithms
  • Audit Trail: Complete calibration history logging
  • Standards: IEC 62304 Class B software
NIST Traceable

Clinical Benefits

Improved Diagnostic Accuracy

Standardised ADC thresholds for PI-RADS scoring with reduced inter-reader variability

Multi-Site Consistency

Enable true quantitative comparison across scanners, sites, and time points

Treatment Monitoring

Track true biological changes in ADC values during active surveillance or therapy

PREDICT Clinical Trial

Study Overview

The PREDICT consortium was awarded a €2.2M Horizon Europe grant to evaluate METRION phantom technology for improved prostate cancer diagnosis.

  • Sites: 5 leading European medical centers
  • Patients: 500 men with suspected prostate cancer
  • Duration: 2024-2026
  • Primary Endpoint: Reduction in unnecessary biopsies
  • Secondary Endpoints: Inter-site ADC consistency, diagnostic confidence

Participating Centers

  • University College London Hospital

    Lead site and protocol development

  • Fraunhofer MEVIS

    AI algorithm development

  • National Physical Laboratory

    Metrological validation

Regulatory Pathway

Current Status: Clinical Trial Phase

METRION is currently undergoing clinical validation as part of the PREDICT trial. The system is classified as a Class IIb medical device in the EU/UK.

MHRA CTN Approved

UK clinical trial authorization granted

FDA 510(k): 2027

Planned US market submission

Join the Future of Quantitative MRI

Be among the first to implement METRION technology at your institution. Join our early access program and help shape the future of diagnostic imaging.