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Not yet recruitingNCT05520229Updated Nov 2, 2022

The Evaluation of a Preanaesthesia Assessment Clinic

An observational study in Preoperative Anaesthesia Clinic, Cancellation Rate and Intraoperative Events, sponsored by University of Agder. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-11-02.

Sponsored by University of Agder · Observational

From the registry’s dates

  • Primary completion was expected by Feb 2023, 3 years 8 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
2,600
Ages
18 Years and older
Sex
All
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Study summary

International evidence highlights the preanaesthetic assessment clinics (PAC) as a system of benefits for both the patient and the anaesthesiologist. The system has gained global acceptance as a routine method of optimising patients' medical conditions prior to surgery and therefore minimising surgery cancellations and improving hospital efficiency. However, a systematic review found no evidence of the efficiency of (PAC) and therefore we wanted to investigate this with the use of hospitals journals.

Read the detailed description

The aim of this study is to evaluate the incidence, causes, and consequences of cancellations, and unanticipated intraoperative events after open or laparoscopic surgery of hemicolectomy patients before and after the implementation of a preoperative anaesthesia assessment clinic (PAC).

The primary outcome is to evaluate the incidence of cancellations and unanticipated intraoperative events after open or laparoscopic surgery of hemicolectomy patients before and after implementation of the preoperative anaesthesia assessment clinic (PAC).

The secondary outcome is to evaluate the patients' characteristics, the main events leading to cancellations and the consequences this brings to the patient and the hospital.

Adverse events reported pre-and post-intervention will be analysed. Patient characteristics will be collected: age, gender, diagnosis, reason and type of surgery, patient admission, assessed in PAC or not, ASA classification (American Society of Anesthesiologist Classification system), who performed the assessment (anaesthetic nurse or anaesthesiologist), type of anaesthesia, former diagnosis/disease with impact on anaesthesia/surgery, present smoker, allergies, blood samples, other examinations, cancellation of surgery, reasons and consequences for cancellations, time of anaesthetic assessment before surgery, intraoperative events, mallampati, Intubation grade, BMI and type of medication.

A specific data collection form will be developed and the data will be collected retrospectively from patient journals.

The number is calculated to: n = 588, n = 294 before and after the implementation of PAC. We use a significance level of 5%. To achieve statistical strength of 80% (beta = 20%), we need 288 patients before and after PAC to detect a difference of at least 10%. Given that we have the opportunity to include many more then we assume that our study has adequate strength. Prevalences of cancellations are estimated as shares and presented with 95% confidence intervals (CIs) calculated using the exact method. Possible differences in background variables in patients included before and after the implementation of PAC will be estimated using kji-square tests or t-tests. The effect of the implementation of PAC will be estimated using logistic regression adjusted for possible confounding factors and results will be presented as adjusted odds ratio (OR) with 95% CI.

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Conditions studied

  • Preoperative Anaesthesia Clinic
  • Cancellation Rate
  • Intraoperative Events
  • Colon Disease

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Keywords

  • Anesthesia, cancellation, pre-operative, clinic, assessment
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In context

Colonic Diseases

142 studies on the registry are indexed under Colonic Diseases; 22 are open to participants now.

This study's planned enrollment of 2,600 is above the median of 170 across 48 observational studies indexed under Colonic Diseases.

Browse Colonic Diseases studies →

Lead sponsor

University of Agder is the lead sponsor of 9 studies on the registry; 1 is open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Patients who have been to surgery for open or laparoscopic partial excision of the intestine.

Inclusion criteria

  • Patients over 18 years old.
  • Open or laparoscopic surgery on elective patients after partial excision of the intestine.
  • Patients following the ERAS (Enhanced recovery after surgery) protocol after the year 2014.
  • Patients who attended PAC after the year 2017 and were assessed by anesthesia staff.

Exclusion criteria

Exclusion Criteria:

  • Emergency patients
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Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
2,600 participants (estimated)
Patient registry
No

Groups and cohorts

  • Pre- Preanaesthesia assessment clinic

    Patients who have been to surgery for an elective laparoscopic or open partial intestine from 2014-2017.

  • Post- Preanaesthesia assessment clinic

    Patients who have been to surgery for an elective laparoscopic or open partial intestine from 2017 and have attended a preanesthesia clinic.

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What researchers measure

Primary outcomes

  1. Cancellation rate, Intraoperative events

    Incidence of Cancellation rate and unanticipated intraoperative events

    Time frame: 2014-2022

Secondary outcomes

  1. Patient's characteristics , cancellation main events and concequenses.

    Patients'characteristics, main events leading to cancellations of surgery, consequenses the cancellations brings to patients and the hospital.

    Time frame: 2014-2022

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 2, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05520229
Lead sponsor
University of Agder
Collaborators
Sorlandet Hospital HF
Responsible party
Eirunn Wallevik Kristoffersen (Principal Investigator, University of Agder) — Principal investigator
First posted
Aug 29, 2022
Start date
Dec 1, 2022 (estimated)
Primary completion
Feb 3, 2023 (estimated)
Completion
Apr 3, 2027 (estimated)
Last update
Nov 2, 2022

Study contacts

Eirunn Kristoffersen, Master
Contact
eirunn.w.kristoffersen@uia.no
+4795207238
Mariann Fossum, Professor
Contact
mariann.fossum@uia.no
+4791854845
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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