- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05740852
Analysis of Risk Factors of Postoperative Pulmonary Infection in Patients With Esophageal Cancer
February 13, 2023 updated by: Xijing Hospital
The goal of this observational study is to learn about in describe participant population. The main questions it aims to answer are:
- What are the risk factors of postoperative pulmonary infection in patients with esophageal cancer?
- Whether we could establish a clinical prediction model to provide basis for early clinical intervention or not? Participants will describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items. If there is a comparison group: Researchers will compare insert groups to see if insert effects.
Study Overview
Status
Completed
Conditions
Detailed Description
Data were collected from the electronic medical records of Xijing Hospital.
Each record is entered by two team members working simultaneously to ensure data accuracy.
Study Type
Observational
Enrollment (Actual)
1688
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
From January 2016 to December 2021, patients with esophageal cancer were hospitalized for surgery in the Department of Gastroenterology, Xijing Hospital.
Description
Inclusion Criteria:
- Diagnosis of esophageal cancer;
- Radical resection of tumor for the first time;
- No distant metastasis was observed in preoperative examination
Exclusion Criteria:
- Patients with preoperative pulmonary infection or symptoms of pulmonary infection;
- Patients with tracheal intubation assisted ventilation before surgery;
- Patients with preoperative lung imaging changes or abnormal white blood cells in blood routine;
- Patients undergoing emergency surgery;
- Patients with other cancers;
- Patients with incomplete clinical data.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Infection
Patients who developed pulmonary infection after radical resection of tumor
|
Without infection
Patients without pulmonary infection after radical resection of tumor
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pneumonia
Time Frame: A week after radical resection of tumor
|
Pulmonary infection in patients with esophageal cancer after radical resection of tumor
|
A week after radical resection of tumor
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2016
Primary Completion (Actual)
October 31, 2021
Study Completion (Actual)
January 31, 2023
Study Registration Dates
First Submitted
February 13, 2023
First Submitted That Met QC Criteria
February 13, 2023
First Posted (Estimate)
February 23, 2023
Study Record Updates
Last Update Posted (Estimate)
February 23, 2023
Last Update Submitted That Met QC Criteria
February 13, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- XijingHCJF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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