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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05637463
Other study ID # 06
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date December 31, 2018

Study information

Verified date October 2022
Source Akdeniz University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


Description:

Background: Postoperative readmission rates of patients have been important indicators in the evaluation of quality service delivery and cost-effectiveness. 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. Material and methods: The research is based on actual patient data in the hospital information management system. In the study, the data of patients who had undergone surgery between January 1, 2018, and December 31, 2018, and presented to the emergency department in the first 90 days after surgery were retrospectively analyzed. Patient data about the date of surgery, type of surgery, department performing the surgery, patient age, gender, type of anesthesia, the length of postoperative hospital stay, date of discharge, date, and reason for presenting to the emergency department, and discharge status (admission, referral, discharge, or death, etc.) recorded on the hospital information management system were evaluated in accordance with "the 18 HIPAA" standards.


Recruitment information / eligibility

Status Completed
Enrollment 620
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Undergone surgery between January 1, 2018, and December 31, 2018, - Presented to the emergency department Exclusion Criteria: • Patients who do not meet the inclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention
no intervention was made

Locations

Country Name City State
Turkey Akdeniz University Antalya

Sponsors (1)

Lead Sponsor Collaborator
Akdeniz University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 Contribute to the strategic planning for quality health service delivery by determining the complaints and repeated admission rates by unit. the reasons for applying complaints on the basis of clinics January 1, 2018, and December 31, 2018,
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