Your Partner for Enrolling and Tracking Patients During a Clinical Trial

The web-based platform to reduce the cost, time, risk, and resources demanded for drug or technology validation by automating data collection, analyzation, and reporting for clinical trials within the orthopedic population.

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91%

Research Patients Reporting Outcomes Preoperatively

94%

Research Patients Reporting Outcomes at 6 Months

84%

Research Patients Reporting Outcomes at 1 Year

4MM

Patient Interactions

90

Presented and Published Research Studies

Key Features

Protocol Development & Regulatory Support

Quickly and efficiently plan and optimize study start up time

Customized Discrete Data Collection

Overcome the challenge of obtaining pain, range of motion, steps, & more through daily tiles and integrations

Standardized & Customized PROMs Collection

Comply with study protocols and reach a higher collection compliance rate for accurate insights to meet study efficacy endpoints with a library of over 200 validated outcome forms

Telemedicine

Enable virtual study visits to engage patients and capture outcomes remotely

Enterprise Dashboards

A customizable portal for real time data insights, variation analysis and evidence-based improvement

E-Consent

Automate the consent process without additional work

Study Track

A portal to easily randomize patients, track recruitment, and monitor ongoing compliance and outcomes

Customized Reporting

Help shape the analysis of your research without additional work

Publication & Abstract Support

Remove the administrative burden of study completion and submission

Recent Clinical Research

Addition of Liposomal Bupivacaine to Adductor Canal Block for Post-operative Pain Following Total Knee Arthroplasty

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A Retrospective Comparison of Functional Outcomes of Robotic-Assisted and Conventional Unicompartmental Knee Arthroplasty

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Tramadol in Knee Osteoarthritis: Does Preoperative Use Affect Patient-Reported Outcomes After Total Knee Arthroplasty?

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Bridge the Outcomes Gap at Your Organization

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