Prediction Models for Risk Score and Prognosis of Intraoperatively Acquired Pressure Injury in Surgical Patients

NCT ID: NCT06166641

Last Updated: 2023-12-12

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

5658 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-08-01

Study Completion Date

2024-12-31

Brief Summary

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The study aims to effectively identify the risk of intraoperative acquired pressure injuries (IAPI) in surgical patients through a prospective multicenter approach. It combines indicators from commonly used assessment tools and practical experience judgments to construct a comprehensive assessment framework.

By incorporating various indicators, the study aims to improve the accuracy and reliability of identifying patients at risk of IAPI during surgery. This will help clinicians in making informed decisions and implementing preventive measures to minimize the occurrence of pressure injuries.

The multicenter approach ensures a diverse and representative sample of patients from different surgical settings. This increases the generalizability of the study findings and enhances the applicability of the assessment framework across various clinical settings.

The project's methodology involves collecting data on patient demographics, medical history, surgical procedure details, and assessment tool scores. These data points will be analyzed to identify significant risk factors for IAPI and develop a risk prediction model.

The study also takes into consideration practical experience judgments, which acknowledge the importance of clinical expertise in assessing patients' risk of IAPI. This ensures that the assessment framework is not solely reliant on assessment tools but also incorporates the insights of experienced clinicians.

Overall, this prospective multicenter study aims to contribute to the field by providing a comprehensive and practical approach to identify the risk of IAPI in surgical patients. The findings from this study can be utilized in clinical practice to improve patient outcomes and reduce the incidence of pressure injuries during surgery.

Detailed Description

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Conditions

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Pressure Ulcer Predictive Models Surgical Patient Clinical Outcome

Keywords

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intraoperatively acquired pressure injury Pressure Ulcer predictive models surgical patient clinical outcome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Intraoperative acquired pressure injury

Intraoperative acquired pressure injury are wounds that develop during a surgical procedure or while a patient is in the operating room. These ulcers are caused by prolonged pressure on a specific area of the body, which reduces blood flow and leads to tissue damage.

Surgical procedure at operating room

Intervention Type PROCEDURE

A surgical procedure in an operating room is a medical intervention that involves making incisions or using minimally invasive techniques to treat a specific condition or perform a diagnostic procedure. The operating room, also known as the operating theater or surgical suite, is a sterile environment specifically designed to minimize the risk of infection and ensure the safety of both the patient and the surgical team.

Interventions

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Surgical procedure at operating room

A surgical procedure in an operating room is a medical intervention that involves making incisions or using minimally invasive techniques to treat a specific condition or perform a diagnostic procedure. The operating room, also known as the operating theater or surgical suite, is a sterile environment specifically designed to minimize the risk of infection and ensure the safety of both the patient and the surgical team.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

Inclusion criteria: All patients who underwent surgery procedure at the participating setting after the study registration.

Exclusion criteria: Patients who have already been diagnosed with pressure injury (stage II and above) before undergoing surgery procedure. Patients/relatives/guardians understand the refusal of data to be used for clinically relevant research. Investigators believe that certain patient conditions may affect the efficacy and safety assessment of this study.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Affiliated Hospital of Guangdong Medical University

OTHER

Sponsor Role lead

Responsible Party

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Yiyue Zhong

Nursing Supervisory

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yiyue Zhong, MD

Role: PRINCIPAL_INVESTIGATOR

Affiliated Hospital of Guangdong Medical University

Locations

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The Affiliated Hospital of Guangdong Medical University

Zhanjiang, Guangdong, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Yiyue Zhong, MD

Role: CONTACT

Phone: 13726909905

Email: [email protected]

Derong Long, BD

Role: CONTACT

Phone: +8613723589749

Email: [email protected]

Facility Contacts

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Wu Jiayuan

Role: primary

References

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Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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PJKT2023-007

Identifier Type: -

Identifier Source: org_study_id