Evaluation of Same-Day Cancellation of Elective Surgeries (DOSCOST)

January 13, 2026 updated by: Sevim Şenol Karataş, Elazıg Fethi Sekin Sehir Hastanesi

Evaluation of the Cancellation of Elective Surgeries on the Day of Operation in Terms of Hospital, Patient, and Cost Outcomes

This study evaluates elective surgeries that were cancelled on the scheduled day of operation. Same-day surgical cancellations may cause emotional stress for patients, inefficient use of hospital resources, and increased health care costs.

The aim of this observational study is to analyze the reasons for same-day cancellations and to assess their impact on patients, hospital workflow, and costs. Patient anxiety levels after cancellation will be evaluated using standardized questionnaires. The findings of this study may help improve perioperative planning and reduce preventable surgical cancellations.

Study Overview

Detailed Description

This prospective observational study was conducted at the operating rooms of Elazığ Fethi Sekin City Hospital. The study included all elective surgical procedures that were cancelled on the scheduled day of operation for any reason after approval by the local ethics committee. Data were collected over a six-month period.

Demographic characteristics of patients, planned surgical procedures, surgical departments, and reasons for cancellation were recorded using patient interviews, medical records, and the hospital information system. Cancellations were categorized as patient-related, hospital-related, or surgery team-related.

The impact of same-day cancellations on hospital resources and costs was evaluated by estimating operating room idle time, personnel costs, unused equipment and medications, bed occupancy, preoperative preparation costs, and additional post-cancellation diagnostic or consultation expenses. Cost calculations were based on official Ministry of Health reimbursement tariffs.

Following cancellation and transfer back to the ward, patients were assessed face to face for anxiety using the State-Trait Anxiety Inventory. The results of this study aim to provide data to improve perioperative planning, optimize hospital resource utilization, and reduce preventable elective surgery cancellations.

This study was registered retrospectively after study completion due to an administrative delay in trial registration.

Study Type

Observational

Enrollment (Actual)

408

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

    • Elaziğ
      • Elâzığ, Elaziğ, Turkey (Türkiye)
        • Fethi Sekin City Hospital

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients scheduled for elective surgery whose procedures were cancelled on the scheduled day of operation at Elazığ Fethi Sekin City Hospital

Description

Inclusion Criteria:

  • Elective surgical procedures cancelled on the scheduled day of operation for any reason.

Exclusion Criteria:

  • Patients who could not be contacted on the day of cancellation.

Patients with insufficient medical or administrative data in their records.

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
Cancelled Elective Surgery Cohort
This cohort includes patients whose elective surgical procedures were cancelled on the scheduled day of operation for any reason.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reasons for same-day cancellation of elective surgeries
Time Frame: From the date of scheduled elective surgery to the end of the same calendar day on which the cancellation occurred, assessed retrospectively using hospital medical records and patient interviews over a 12-month study period.
Categorization of cancellation reasons as patient-related, hospital-related, or surgical team-related based on medical records and patient interviews.
From the date of scheduled elective surgery to the end of the same calendar day on which the cancellation occurred, assessed retrospectively using hospital medical records and patient interviews over a 12-month study period.
Estimated hospital cost associated with cancelled elective surgeries
Time Frame: Perioperative / Periprocedural
Total estimated cost including operating room idle time, personnel costs, unused equipment and medications, bed occupancy, preoperative preparation costs, and additional post-cancellation diagnostic or consultation expenses.
Perioperative / Periprocedural

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
State anxiety level after surgical cancellation (STAI-State score)
Time Frame: Within 24 hours after cancellation
The State Anxiety subscale of the State-Trait Anxiety Inventory (STAI-State) is a validated self-report scale ranging from 20 to 80, with higher scores indicating greater levels of anxiety.
Within 24 hours after cancellation

Collaborators and Investigators

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

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)

March 25, 2025

Primary Completion (Actual)

December 1, 2025

Study Completion (Actual)

December 10, 2025

Study Registration Dates

First Submitted

December 18, 2025

First Submitted That Met QC Criteria

January 13, 2026

First Posted (Actual)

January 22, 2026

Study Record Updates

Last Update Posted (Actual)

January 22, 2026

Last Update Submitted That Met QC Criteria

January 13, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Preoperative Anxiety

Subscribe