Phase studies

ePRO, eCOA and EDC

ePRO, eCOA, and EDC - or a link to the EDC you already have. Live dashboards, ready in under four weeks.

Patients

863

9 reporting clinics

6-month improvement

31

Mean outcome score

Follow-up complete

95%

Across due timepoints

Safety flags

4

Awaiting review

Patient Reported Outcomes

Pain, stiffness, and function · Lower is better · Mean score for 863 patients · 31 point improvement

TimingBaseline
Date12 Jan 2026

Total60/96
Pain13/20
Stiffness5/8
Function42/68

Patients by clinic

Enrolment in the selected cohort

  • Manchester Orthopaedics248
  • Berlin Gelenkzentrum173
  • Paris Clinique du Mouvement156
  • Bristol Joint Centre104
  • Hamburg Movement Lab67
  • Bordeaux Foot Institute52
  • London Sports Clinic31
  • Munich Ortho Campus18
  • Lyon Outcomes Centre14

Anatomic areas

5 areas · 863 procedures

  • Knee605
  • Shoulder87
  • Ankle82
  • Hip69
  • Spine20

Procedures by area

Events in the selected cohort

  • Knee605
  • Shoulder87
  • Ankle82
  • Hip69
  • Spine20

Filters update outcomes, completion, clinic benchmarking, and safety signals together.

Aggregated, pseudonymised sponsor view

Start with the sponsor dashboard, then the site workspace and the patient diary.

What this covers

Built for the study budget you actually have

ePRO is what the patient reports. eCOA is the wider set of clinical outcome assessments, including what the clinician records. EDC is the system that holds the study data. You can use all three here, or keep your EDC and use Patient Watch for the outcomes.

Lower budgets

EDC we can provide when a full enterprise system is more than the study needs.

Integrate or export

ePRO and eCOA can feed the EDC you already use, or leave as files.

.csv, .xlsx, SAS, R

The formats statisticians and data managers already open.

Always live

Dashboards update as patients and sites submit. You do not wait for a lock to see the study.

<4 weeks

Typical configuration time, from agreed instruments and schedule to a study you can open.

How it works

Integrate, or export. The dashboard stays live.

EDC for a lower budget

Electronic data capture for phase studies that cannot carry a large EDC contract. Structured forms, schedules, and an audit trail, scoped to the study.

ePRO and eCOA into your EDC

Patient-reported outcomes (ePRO) and clinician outcome assessments (eCOA) can integrate with the EDC you already run, so sites are not asked to type the same answers twice.

Or take the data with you

When integration is not the path, export CSV, Excel (.xlsx), SAS, and R. The same dataset your biostatistics team expects.

Live dashboards either way

Recruitment, completion, and scores stay on dashboards while the study is running. Exports are a copy. The dashboard is the live view.

Configured in under four weeks

Instruments, visit windows, reminders, and roles are usually in place in under four weeks, once the protocol points are agreed.

One capture, two audiences

Patients complete outcomes in their own language. Sites see what is due. Sponsors see the cohort without chasing spreadsheets.

Scope the next phase study

Tell us the phase, the endpoints, and whether you need EDC or an integration. We will say what fits in under four weeks.