- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07357753
Evaluation of Same-Day Cancellation of Elective Surgeries (DOSCOST)
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
Status
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Elaziğ
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Elâzığ, Elaziğ, Turkey (Türkiye)
- Fethi Sekin City Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Cancelled Elective Surgery Cohort
This cohort includes patients whose elective surgical procedures were cancelled on the scheduled day of operation for any reason.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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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.
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Categorization of cancellation reasons as patient-related, hospital-related, or surgical team-related based on medical records and patient interviews.
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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.
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Estimated hospital cost associated with cancelled elective surgeries
Time Frame: Perioperative / Periprocedural
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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.
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Perioperative / Periprocedural
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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.
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Within 24 hours after cancellation
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- FSCH-OR-CANCEL-2025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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