ClinicalTrials.gg
CompletedNCT07780526Updated Oct 20, 2026

Pilot Study of Anesthesiologists' Preoperative Prediction of Postoperative Intensive Care Unit Admission

An observational study in Postoperative Intensive Care Unit Admission and Perioperative Risk Assessment, sponsored by Van Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Van Training and Research Hospital · Observational

Updated Oct 20, 2026Now CompletedStart date moved+3 moreGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
114
Ages
18 Years and older
Sex
All
01

Study summary

This prospective observational pilot study will evaluate how accurately anesthesiologists can predict, before a procedure, whether an adult patient will require admission to an intensive care unit (İCU) after surgery or an endoscopic procedure.

Before each procedure, the anesthesiologist will record whether postoperative intensive care unit (İCU) care is expected and the clinical factors influencing this assessment. No changes will be made to the patient's usual medical care. After the procedure, the researchers will record whether the patient was admitted to the İCU and whether the admission was planned or unplanned. Additional information, including İCU and hospital length of stay, need for organ support, and in-hospital mortality, will also be collected when applicable.

The pilot study will also assess whether the planned data collection process is practical and whether the required study information can be collected completely before conducting the main prospective study.

02

Conditions studied

  • Postoperative Intensive Care Unit Admission
  • Perioperative Risk Assessment
03

In context

Lead sponsor

Van Training and Research Hospital is the lead sponsor of 8 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will consist of adult patients undergoing eligible surgical or endoscopic procedures in the participating operating rooms and endoscopy units on the predefined study days. Patients with The american society of anesthesiologists (ASA) Physical Status of I-II will be included if they undergo a major procedure, while patients with ASA Physical Status of III-V will be considered for inclusion regardless of procedural magnitude, provided that all other eligibility criteria are met. Preoperative clinical assessment will be completed before the procedure, and postoperative outcomes will be recorded prospectively.

Eligibility criteria

İnclusion Criteria:

  • Age 18 years or older.
  • Undergoing an eligible surgical or endoscopic procedure on a predefined study day.
  • The (ASA) Physical Status of I-II and undergoing a major surgical or endoscopic procedure, or ASA Physical Status of III-V and undergoing an eligible surgical or endoscopic procedure.
  • Preoperative anesthesiology assessment completed before the procedure.

Exclusion Criteria:

  • Age younger than 18 years.
  • ASA Physical Status of I-II and undergoing a minor or non-major procedure.
  • Undergoing cardiac surgery.
  • Already admitted to an intensive care unit before the index procedure.
  • The planned surgical or endoscopic procedure is not ultimately performed.
  • The required preoperative assessment cannot be completed before the procedure.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
114 participants (actual)
Patient registry
No

Groups and cohorts

  • Adult Surgical and Endoscopic Procedure Cohort

    Adult patients undergoing eligible surgical or endoscopic procedures on the predefined study days will be included in this prospective observational cohort. Before each procedure, the anesthesiologist will record whether postoperative intensive care unit admission is anticipated. Actual intensive care unit (İCU) admission and other postoperative outcomes will subsequently be recorded. No study-specific intervention will be performed.

    Other: Preoperative Clinical Prediction of Postoperative ICU Admission

Interventions

  • OtherPreoperative Clinical Prediction of Postoperative ICU Admission

    Before the index procedure, the anesthesiologist will record whether postoperative intensive care unit admission is anticipated based on routine preoperative clinical assessment. This assessment is observational and will not alter routine patient care.

06

What researchers measure

Primary outcomes

  1. Accuracy of Preoperative Prediction of Postoperative Intensive Care Unit Admission

    Overall prediction accuracy will be calculated as the proportion of evaluable patients for whom the anesthesiologist's preoperative prediction of postoperative intensive care unit (İCU) need agrees with actual İCU admission status within 24 hours after the index procedure. Patients with mandatory postoperative İCU admission according to institutional protocol will not be included in this primary analysis.

    Time frame: Within 24 hours after the index surgical or endoscopic procedure

Secondary outcomes

  1. Unanticipated Postoperative Intensive Care Unit Admission

    The proportion of evaluable patients who are admitted to the intensive care unit (İCU) within 24 hours after the index procedure despite postoperative İCU care not being anticipated during the preoperative anesthesiology assessment.

    Time frame: Within 24 hours after the index surgical or endoscopic procedure

07

Study locations

1 site
  • Van Education and Research Hospital
    Van, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Oct 20, 2026
Start date
Aug 17, 2026→Aug 15, 2026 (actual)
Oct 20, 2026
Primary completion
Aug 29, 2026→Aug 30, 2026 (actual)
Oct 20, 2026
Study completion
Sep 5, 2026→Sep 10, 2026 (actual)
Oct 20, 2026
Enrollment
100 (estimated)→114 (actual)
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    Recruiting→Completed
    Start date Aug 17, 2026→Aug 15, 2026 (now actual)
    Primary completion Aug 29, 2026→Aug 30, 2026 (now actual)
    Study completion Sep 5, 2026→Sep 10, 2026 (now actual)
    Enrollment 100 (estimated)→114 (actual)
    + 3 other changes: verification date, contact details and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07780526
Lead sponsor
Van Training and Research Hospital
Responsible party
Halide Aydin (anesthesiology specialist, principal investigator, Van Training and Research Hospital) — Principal investigator
First posted
Aug 21, 2026
Start date
Aug 15, 2026
Primary completion
Aug 30, 2026
Completion
Sep 10, 2026
Last update
Oct 20, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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