NCT05671952

Brief Summary

The purpose of this study is to carry out demonstrative comprehensive intervention for elderly patients in several hospitals to observe whether it can reduce the incidence and mortality of perioperative pulmonary complications in elderly patients and improve their perioperative prognosis.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
5,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2023

Shorter than P25 for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2023

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

January 2, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 5, 2023

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2023

Completed
Last Updated

January 5, 2023

Status Verified

December 1, 2022

Enrollment Period

4 months

First QC Date

January 2, 2023

Last Update Submit

January 3, 2023

Conditions

Postoperative Pulmonary Complications

Outcome Measures

Primary Outcomes (1)

  • Postoperative pulmonary complications

    within one week after surgery

Secondary Outcomes (1)

  • Postoperative pulmonary complications

    30 days after surgery

Study Arms (2)

intervention group

EXPERIMENTAL

Application of integrated intervention system programs

Other: Application of integrated intervention system programs

Control group

NO INTERVENTION

No intervention

Interventions

Application of integrated intervention system programsOTHER

Application of integrated intervention system programs

intervention group

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • age 65 years or older
  • receiving invasive ventilation during general anesthesia for surgery

You may not qualify if:

  • preoperative mechanical ventilation
  • procedures related to a previous surgical complication
  • a second operation after surgery
  • organ transplantation
  • discharged within 24 hours after surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 2, 2023

First Posted

January 5, 2023

Study Start

January 1, 2023

Primary Completion

May 1, 2023

Study Completion

May 1, 2023

Last Updated

January 5, 2023

Record last verified: 2022-12