Postoperative Pulmonary Complications Between Patients Undergoing Abdominal Surgery in Plateau and Plain Areas

NCT ID: NCT05131009

Last Updated: 2021-11-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

600 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-11-30

Study Completion Date

2022-09-30

Brief Summary

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This study aims to collect perioperative diagnosis and treatment information of patients undergoing abdominal surgery at plateau and plain areas , collect blood and others samples for laboratory testing when necessary, analyzing the data to clarify the incidence and risk factors of pulmonary complications in patients undergoing abdominal surgery at different altitudes, so as to reduce the risk of pulmonary complications and even death in clinical practice.

Detailed Description

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Conditions

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Postoperative Pulmonary Complications;Abdominal Surgery

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with pulmonary complications following abdominal surgery

No interventions assigned to this group

Patients without pulmonary complications following abdominal surgery

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. ≥ 18 years old;
2. scheduled for elective abdominal surgery under general anesthesia;
3. ASAⅠ-Ⅲ

Exclusion Criteria

1. Patients and their family members refused to be enrolled;
2. patients were unable to communicate because of language disorders such as dementia and hearing impairment;
3. patients were admitted to ICU 48 hours before operation;
4. preoperative diagnosis of ARDS, aspiration pneumonia, pulmonary embolism or pulmonary edema or other acute respiratory diseases;
5. mechanical ventilation within one week before operation;
6. death or discharge within 24 hours after operation;
7. second operation due to postoperative complications
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Qinghai People's Hospital

OTHER

Sponsor Role collaborator

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

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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

Wuhan, Hubei, China

Site Status

Countries

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China

Central Contacts

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Qingping Wu, Professor

Role: CONTACT

Phone: 13971605283

Email: [email protected]

Facility Contacts

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Qingping Wu

Role: primary

Other Identifiers

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PPC202108

Identifier Type: -

Identifier Source: org_study_id