Factors Affecting Surgical Recovery in Hospital Patients

October 29, 2024 updated by: Second Affiliated Hospital of Wenzhou Medical University

A Comprehensive Analysis of Factors Influencing Adverse Postoperative Outcomes in Hospitalized Surgical Patients

The objective of this observational study is to elucidate the factors influencing adverse postoperative outcomes in hospitalized surgical patients. The primary questions addressed are:

What factors contribute to the occurrence of adverse outcomes following surgery? How can the risks be mitigated to achieve improved postoperative outcomes?

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

600

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • China
    • Zhejiang
      • Wenzhou, Zhejiang, China, 325027
        • The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University,

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

Adult patients of all inpatient surgeries conducted at a major comprehensive hospital.

Description

Inclusion Criteria:

  • The study population consisted of all patients who had undergone surgery, with no instances of severe data missingness.

Exclusion Criteria:

  • Missing data were identified where the rate of missingness was greater than 20%

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
Intervention / Treatment
The favourable outcomes group
Procedure: surgery time
This study is a retrospective observational study, with surgery time being one of the exposure factors under investigation.
Procedure: surgeon
This study is a retrospective observational study, with surgeon being one of the exposure factors under investigation.
Procedure: surgical procedure duration
This study is a retrospective observational study, with surgical procedure duration being one of the exposure factors under investigation.
Procedure: operating room
This study is a retrospective observational study, with surgical procedure duration being one of the exposure factors under investigation.
Procedure: type of surgery
This study is a retrospective observational study, with type of surgery being one of the exposure factors under investigation.
The poor outcomes group
Procedure: surgery time
This study is a retrospective observational study, with surgery time being one of the exposure factors under investigation.
Procedure: surgeon
This study is a retrospective observational study, with surgeon being one of the exposure factors under investigation.
Procedure: surgical procedure duration
This study is a retrospective observational study, with surgical procedure duration being one of the exposure factors under investigation.
Procedure: operating room
This study is a retrospective observational study, with surgical procedure duration being one of the exposure factors under investigation.
Procedure: type of surgery
This study is a retrospective observational study, with type of surgery being one of the exposure factors under investigation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Death
Time Frame: 1 year
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Second Affiliated Hospital of Wenzhou Medical University

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)

September 1, 2024

Primary Completion (Actual)

October 1, 2024

Study Completion (Actual)

October 17, 2024

Study Registration Dates

First Submitted

July 3, 2024

First Submitted That Met QC Criteria

July 14, 2024

First Posted (Actual)

July 16, 2024

Study Record Updates

Last Update Posted (Actual)

October 31, 2024

Last Update Submitted That Met QC Criteria

October 29, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • SAHoWMU-CR2024-16-211

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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