Providing Standardized Consented PROMs (Patient Reported Outcome Measures) for Improving Pain Treatment
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Pain Postoperative
- Design
- Observational Model: CohortTime Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
In order to reach this objective, a non-interventional prospective data collection aiming at reaching a consensus on a core set of PROMs which reliably predict and/or measure success in acute and chronic pain treatments in real life conditions and identifying predictors for chronification of postope...
In order to reach this objective, a non-interventional prospective data collection aiming at reaching a consensus on a core set of PROMs which reliably predict and/or measure success in acute and chronic pain treatments in real life conditions and identifying predictors for chronification of postoperative pain will be conducted (PROMPT NIT-1). Aim of the data collection is to evaluate the abilities of certain PROMs in assessing acute post-surgical pain outcomes in daily routine care of patients after four different surgical procedures: (total knee replacement, breast surgery, sternotomy and surgery related to endometriosis), and to validate selected risk factors for chronification prospectively.
Tracking Information
- NCT #
- NCT03834922
- Collaborators
- University Hospital Muenster
- Grünenthal GmbH
- Hospital Ambroise Paré Paris
- Novartis Pharmaceuticals
- Hôpital Raymond Poincaré
- University of Helsinki
- Infirmerie Protestante Lyon
- University Hospital St Luc, Brussels
- Oxford University Hospitals NHS Trust
- University Hospital, Geneva
- Hospital Clínico Universitario de Valladolid
- Cancer Center Porto, Portugal
- Barts & The London NHS Trust
- Orthopedic Center Santy, Lyon, France
- University of Homburg
- University Hospital Bergmannsheil Bochum
- University of Naples
- University Hospital Inselspital, Berne
- Orthopedic Institute Banjika, Belgrade, Serbia
- Cardiovascular Center Dedinje, Belgrade, Serbia
- University Hospital Dresden
- Investigators
- Study Chair: Winfried Meissner, Prof. Jena University Hospital Study Chair: Hiltrud Liedgens, Dr. Grünenthal GmbH Principal Investigator: Esther Pogatzki-Zahn, Prof. University Hospital Münster Principal Investigator: Dominique Fletcher, Prof. Hospital Ambroise Paré Paris Principal Investigator: Shaloo Pandhi Novartis
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