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Elective Surgery CancellationDOSCOSTNCT07357753

Evaluation of Same-Day Cancellation of Elective Surgeries

An observational study of Elective Surgery Cancellation and Preoperative Anxiety, run by Elazıg Fethi Sekin Sehir Hastanesi at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Any age
How many people
408 participants
Where
1 siteTurkey (Türkiye)
Study dates
25 Mar 2025to 10 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

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

Who may be able to join

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

Who cannot join

  • Patients who could not be contacted on the day of cancellation.
  • Patients with insufficient medical or administrative data in their records.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Fethi Sekin City Hospital

    Elâzığ, Elaziğ

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Read the 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.

Keywords
Elective surgery cancellation, Cancellation reasons, Healthcare costs, Economic impact, Patient anxiety

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07357753
Study groupRoleWhat they receive
Cancelled Elective Surgery CohortThis cohort includes patients whose elective surgical procedures were cancelled on the scheduled day of operation for any reason.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Reasons for same-day cancellation of elective surgeries

    Categorization of cancellation reasons as patient-related, hospital-related, or surgical team-related based on medical records and patient interviews.

    Measured: 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.

  2. Estimated hospital cost associated with cancelled elective surgeries

    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.

    Measured: Perioperative / Periprocedural

Secondary outcomes (1)
  1. State anxiety level after surgical cancellation (STAI-State score)

    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.

    Measured: Within 24 hours after cancellation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jan 2026
  2. Study start25 Mar 2025
  3. Primary completion1 Dec 2025
  4. Study completion10 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
408 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07357753
Sponsor's protocol ID
FSCH-OR-CANCEL-2025
Acronym
DOSCOST
Status last verified
Jan 2026
First submitted
18 Dec 2025
Last updated
22 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Elective Surgery Cancellation and Preoperative Anxiety, run by Elazıg Fethi Sekin Sehir Hastanesi at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jan 2026.

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