Prospective data collection based on EndoCert questionnaires for the outcomes and quality of life of patients who have undergone arthroplasty – a multicenter study

Prospective data collection based on EndoCert questionnaires for the outcomes and quality of life of patients who have undergone arthroplasty – a multicenter study - PREM vs. PROM

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033383

Enrollment

1250

Registered

2024-01-09

Start date

2023-07-23

Completion date

Unknown

Last updated

2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M16 M17

Interventions

Group 1: A questionnaire concept has been developed, consisting of multiple scores and quality-related questions. The questionnaires include the EndoCert Risk Score, joint-specific Oxford Score, quali

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Indication for primary hip arthroplasty Indication for primary knee arthroplasty Indication for revision of a hip arthroplasty Indication for revision of a knee arthroplasty

Exclusion criteria

Exclusion criteria: Fractures and Tumor Surgeries

Design outcomes

Primary

Measure	Time frame
- Oxford Score (=PROMs) - EuroQol-5D Score (= quality of life) - EndoCert-Riskscore (=PROMs, Net Promoter Score) - Patients' Experience Questionnaire (PEQ=PREMs) - Complications (according to EndoCert), re-interventions - Length of hospital stay	—

Secondary

Measure	Time frame
patient-specific risk factors, Pain symptoms, reasons for revision Center comparison	—

Countries

Germany

Contacts

Public ContactKatrin Osmanski-Zenk

Orthopädische Klinik und Poliklinik der Universitätsmedizin Rostock

katrin.osmanski-zenk@med.uni-rostock.de+493814949318

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026