Effects of Volatile Anaesthetics on Incidence of Postoperative Depression and Anxiety in Elderly Patients

NCT06307717 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8000

Last updated 2024-04-10

No results posted yet for this study

Summary

This study is a retrospective analysis of a large-scale multicentre prospective cohort study that investigates the impact of volatile anaesthetics on the incidence of postoperative depression and anxiety among elderly patients.

Conditions

  • Cohort Studies

Interventions

DRUG

volatile anaesthetic (sevoflurane, isoflurane, desflurane)

Patients receiving volatile anaesthetics received at least one volatile anaesthetic (sevoflurane, isoflurane, desflurane), and those who received non-volatile anaesthetics did not receive any volatile anaesthetic.

Sponsors & Collaborators

  • Beijing Tsinghua Changgeng Hospital

    collaborator OTHER
  • Peking University First Hospital

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

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Beijing Anzhen Hospital

    collaborator OTHER
  • Central South University

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Zhejiang University

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • The Affiliated Hospital Of Guizhou Medical University

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • Taihe Hospital

    collaborator OTHER
  • Chinese PLA General Hospital

    lead OTHER

Principal Investigators

  • WEIDONG MI, PhD · Chinese PLA General Hospital

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-04-01
Primary Completion
2021-10-31
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 NCT06307717 on ClinicalTrials.gov