Effect of Dexmedetomidine on Postoperative Mental Disorders and Long-term Survival in Elderly Patients

NCT06362408 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 6000

Last updated 2024-11-04

No results posted yet for this study

Summary

China's aging population is causing an increase in the number of senior persons undergoing surgery. More and more clinicians are paying attention to the postoperative survival and mental health of elderly surgical patients.

Dexmedetomidine (DEX) is an alpha-2 adrenergic agonist that works by inhibiting norepinephrine releasing renaline, which reduces inflammation and thus plays a protective role in the central nervous system. DEX has the potential to prevent and treat postoperative anxiety and depression in elderly patients undergoing non-cardiac surgery.

Further exploration of evidence for evidence-based medicine is needed. Based on the above research background, this hypothesis is proposed: in elderly patients undergoing noncardiac surgery, intraoperative DEX is associated with a reduction in short-term postoperative mental disorders and a reduction in long-term postoperative mortality.

Conditions

  • Cohort Studies

Interventions

DRUG

Dexmedetomidine

Older patients who have used dexmedetomidine(safe use range: 0.2\~1.0 μg/(kg·h)) for anesthesia induction or maintenance during surgery were classified as the DEX group. On the contrary, patients who did not use dexmedetomidine throughout the entire anesthesia process were identified as the Non-DEX group.

Sponsors & Collaborators

  • Beijing Tiantan Hospital

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • The Affiliated Hospital Of Guizhou Medical University

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

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

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • The First Xiangya Hospital of Central South University

    collaborator UNKNOWN
  • Second Xiangya Hospital of Central South University

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Chinese PLA General Hospital

    lead OTHER

Principal Investigators

  • WEIDONG MI, PhD · Chinese PLA General Hospital

Eligibility

Min Age
65 Years
Max Age
110 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-01
Primary Completion
2023-05-25
Completion
2023-06-01

Countries

  • China

Study Locations

More Related Trials

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 NCT06362408 on ClinicalTrials.gov