Providing Standardized Consented PROMs (Patient Reported Outcome Measures) for Improving Pain Treatment

Summary

PROMPT aims at improving management of acute and chronic pain by identifying a core set of PROMs (patient reported outcome measures) that are predictive indicators of treatment success in clinical practice and controlled trials. These will not only address pain intensities as well as the functional consequences of pain for individuals but also identify patients at risk of experiencing chronification of acute post-operative pain. Results will help health care professionals to individualize pain management, and thus improve the quality of life of pain patients.

Conditions

• Pain, Postoperative

Interventions

OTHER

Prospective data collection

No intervention. It's a prospective data collection.

Sponsors & Collaborators

• Grünenthal GmbH

  collaborator INDUSTRY

• University Hospital Muenster

  collaborator OTHER

• Hospital Ambroise Paré Paris

  collaborator OTHER

• Novartis Pharmaceuticals

  collaborator INDUSTRY

• Hôpital Raymond Poincaré

  collaborator OTHER

• University of Helsinki

  collaborator OTHER

• University Hospital St Luc, Brussels

  collaborator OTHER

• Oxford University Hospitals NHS Trust

  collaborator OTHER

• University Hospital, Geneva

  collaborator OTHER

• Orthopedic Center Santy, Lyon, France

  collaborator UNKNOWN

• University of Naples

  collaborator OTHER

• Hospital Clínico Universitario de Valladolid

  collaborator OTHER

• Cancer Center Porto, Portugal

  collaborator UNKNOWN

• Orthopedic Institute Banjika, Belgrade, Serbia

  collaborator UNKNOWN

• Cardiovascular Center Dedinje, Belgrade, Serbia

  collaborator UNKNOWN

• University of Homburg

  collaborator OTHER

• Barts & The London NHS Trust

  collaborator OTHER

• Insel Gruppe AG, University Hospital Bern

  collaborator OTHER

• University Hospital Dresden

  collaborator OTHER

• University Hospital Bergmannsheil Bochum

  collaborator OTHER

• Infirmerie Protestante de Lyon

  collaborator OTHER

• Prof. Dr. Winfried Meissner

  lead OTHER

Principal Investigators

• Winfried Meissner, Prof. · Jena University Hospital

• Hiltrud Liedgens, Dr. · Grünenthal GmbH

• Esther Pogatzki-Zahn, Prof. · University Hospital Münster

• Dominique Fletcher, Prof. · Hospital Ambroise Paré Paris

• Shaloo Pandhi · Novartis

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2019-09-24

Primary Completion

2022-06-30

Completion

2022-06-30

Countries

• Germany

Study Locations