Clinical Prediction Model and External Validation of Chronic Postsurgical Pain in Elders

NCT05372406 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7770

Last updated 2022-05-25

No results posted yet for this study

Summary

This study will collect perioperative pain-related data of elderly patients in multi-centers. Analyzing these collected data to find the high-risk factors of chronic postsurgical pain in elderly patients and to establish an early-warning models of perioperative pain in elderly patients, so as to improve the ability of assessing the risks of postoperative pain in elderly patients and providing an early warning.

Based on the database, the investigators intend to explore:

* Perioperative risk assessment methods and early warning models for elderly patients;
* Practical, safe, and effective risk prevention and control system through subsequent studies.

Conditions

  • Chronic Postsurgical Pain

Interventions

OTHER

• no intervention

• no intervention

Sponsors & Collaborators

  • The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • The Affiliated Hospital Of Guizhou Medical University

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Chinese PLA General Hospital

    lead OTHER

Principal Investigators

  • Mi Weidong, PhD · Chinese PLA General Hospital

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-04-01
Primary Completion
2022-04-30
Completion
2022-04-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05372406 on ClinicalTrials.gov