NCT05637463

Brief Summary

The objective of this study was conducted to examine the reasons for patients' utilization of the emergency department and the rates of readmission in the first 90 days after surgery.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
620

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2018

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

Study Start

First participant enrolled

January 1, 2018

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2018

Completed
3.9 years until next milestone

First Submitted

Initial submission to the registry

November 23, 2022

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 5, 2022

Completed
Last Updated

December 5, 2022

Status Verified

October 1, 2022

Enrollment Period

12 months

First QC Date

November 23, 2022

Last Update Submit

December 2, 2022

Conditions

SurgeryNursing Caries

Keywords

Surgery,emergency department,readmission

Outcome Measures

Primary Outcomes (1)

  • Identify the causes of preventable post-operative emergency utilization

    the reasons for patients' utilization of the emergency department after surgery

    January 1, 2018, and December 31, 2018,

Secondary Outcomes (1)

  • Contribute to the strategic planning for quality health service delivery by determining the complaints and repeated admission rates by unit.

    January 1, 2018, and December 31, 2018,

Interventions

No interventionOTHER

no intervention was made

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The population of the study consisted of 1705 patients who had undergone surgery between January 1, 2018 and December 31, 2018 and presented to the emergency department within the first 90 days after discharge.

You may qualify if:

  • Undergone surgery between January 1, 2018, and December 31, 2018,
  • Presented to the emergency department

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Akdeniz University

Antalya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Fatma CEBECİ

    Akdeniz University

    STUDY DIRECTOR

  • Songül Bişkin Çetin

    Akdeniz University

    PRINCIPAL INVESTIGATOR

  • Volkan Doğru

    Akdeniz University

    PRINCIPAL INVESTIGATOR

  • Mustafa Coşkun

    Akdeniz University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

November 23, 2022

First Posted

December 5, 2022

Study Start

January 1, 2018

Primary Completion

December 31, 2018

Study Completion

December 31, 2018

Last Updated

December 5, 2022

Record last verified: 2022-10

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)