NCT06502600

Brief Summary

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?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
600

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 3, 2024

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 16, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2024

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 17, 2024

Completed
Last Updated

October 31, 2024

Status Verified

October 1, 2024

Enrollment Period

1 month

First QC Date

July 3, 2024

Last Update Submit

October 29, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Death

    1 year

Study Arms (2)

The favourable outcomes group

Procedure: surgery timeProcedure: surgeonProcedure: surgical procedure durationProcedure: operating roomProcedure: type of surgery

The poor outcomes group

Procedure: surgery timeProcedure: surgeonProcedure: surgical procedure durationProcedure: operating roomProcedure: type of surgery

Interventions

surgery timePROCEDURE

This study is a retrospective observational study, with surgery time being one of the exposure factors under investigation.

The favourable outcomes groupThe poor outcomes group
surgeonPROCEDURE

This study is a retrospective observational study, with surgeon being one of the exposure factors under investigation.

The favourable outcomes groupThe poor outcomes group

This study is a retrospective observational study, with surgical procedure duration being one of the exposure factors under investigation.

The favourable outcomes groupThe poor outcomes group

This study is a retrospective observational study, with surgical procedure duration being one of the exposure factors under investigation.

The favourable outcomes groupThe poor outcomes group

This study is a retrospective observational study, with type of surgery being one of the exposure factors under investigation.

The favourable outcomes groupThe poor outcomes group

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University,

Wenzhou, Zhejiang, 325027, China

Location

Related Publications (1)

  • Xie M, Zhou Z, Fei F, Deng Y, Liu C, Jin W, Chen F, Wang L, Chen C, Wang Z, Weng J, Xu Z. Risk assessment models for venous thromboembolism in surgical inpatients: a multicenter retrospective cohort study. Eur J Med Res. 2025 Nov 27;30(1):1298. doi: 10.1186/s40001-025-03575-3.

MeSH Terms

Interventions

Operative TimeSurgeonsOperating Rooms

Intervention Hierarchy (Ancestors)

Intraoperative PeriodPerioperative PeriodSurgical Procedures, OperativePatient CareHealth ServicesHealth Care Facilities Workforce and ServicesPhysiciansHealth PersonnelHospital UnitsHealth Facilities

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 3, 2024

First Posted

July 16, 2024

Study Start

September 1, 2024

Primary Completion

October 1, 2024

Study Completion

October 17, 2024

Last Updated

October 31, 2024

Record last verified: 2024-10

Locations