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Multi-center Study on Reducing Postoperative Pulmonary Complications in Elderly Patients

H

Huazhong University of Science and Technology

Status

Not yet enrolling

Conditions

Postoperative Pulmonary Complications

Treatments

Other: Application of integrated intervention system programs

Study type

Interventional

Funder types

Other

Identifiers

NCT05671952
PPC20221203

Details and patient eligibility

About

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.

Full description

This study investigated the incidence of postoperative pulmonary complications in various hospitals, and carried out demonstrative comprehensive intervention for elderly patients in several hospitals according to the comprehensive intervention system program of perioperative pulmonary complications, to observe whether the perioperative prognosis can be improved and the quality of life can be improved, thus verifying and optimizing the current evaluation system and intervention system, and providing evidence support for further extensive application.

Enrollment

5,000 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. age 65 years or older
  2. receiving invasive ventilation during general anesthesia for surgery

Exclusion criteria

  1. preoperative mechanical ventilation
  2. procedures related to a previous surgical complication
  3. a second operation after surgery
  4. organ transplantation
  5. discharged within 24 hours after surgery

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

5,000 participants in 2 patient groups

intervention group
Experimental group
Description:
Application of integrated intervention system programs
Treatment:
Other: Application of integrated intervention system programs
Control group
No Intervention group
Description:
No intervention

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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