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Not yet recruitingNCT07895199IPOSUpdated Oct 26, 2026

The Irish Perioperative OutcomeS (IPOS) Study

An observational study in Outcomes Following Major Surgery in Older Adults, sponsored by University College Hospital Galway. Not yet recruiting. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by University College Hospital Galway · Observational

Updated Oct 26, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
60 Years and older
Sex
All
01

Study summary

The Irish Perioperative OutcomeS (IPOS) Study aims to better understand the factors that influence recovery and outcomes in older adults undergoing major surgery in Ireland. As people live longer and more individuals have multiple long-term health conditions, increasing numbers of older patients require surgical treatment. These patients may be at greater risk of complications after surgery, including infections, heart problems, delirium (confusion), admission to intensive care, and death.

This study will collect information from routine medical records of patients aged 60 years and older who undergo major planned or emergency surgery in participating hospitals across Ireland. No changes will be made to patients' treatment or care, and no additional tests or procedures will be performed as part of the study.

Researchers will examine patient characteristics, health conditions, frailty, surgical factors, postoperative complications, and the level of care patients receive after surgery. The study will also evaluate whether access to critical care services and other healthcare resources affects outcomes.

The information gathered will help identify factors associated with better and worse surgical outcomes and may highlight opportunities to improve perioperative care for older patients. Findings from the study are expected to support healthcare planning, resource allocation, and quality improvement initiatives aimed at improving the safety and outcomes of surgery for older adults in Ireland.

Read the detailed description

The Irish Perioperative OutcomeS (IPOS) Study is a national, multicentre, prospective observational cohort study designed to characterize perioperative risk, resource utilization, and clinical outcomes among older adults undergoing major inpatient surgery in Ireland.

Advances in perioperative medicine and surgical techniques have enabled increasing numbers of older patients with multiple comorbidities to undergo complex surgical procedures. However, older surgical patients remain at increased risk of postoperative complications, including pneumonia, sepsis, cardiac events, delirium, unplanned intensive care unit (ICU) admission, and mortality. Despite international evidence describing these risks, there is limited contemporary national data regarding perioperative risk profiles, adverse outcomes, and healthcare capacity within the Irish healthcare system.

The IPOS Study will recruit consecutive eligible patients aged 60 years and older undergoing major elective surgery requiring hospital admission or emergency surgery at participating hospitals throughout Ireland. Patients undergoing planned day-case procedures, cardiac surgery, neurosurgery, obstetric procedures, or radiological interventions will be excluded.

This is a non-interventional study. Data will be collected prospectively from routinely recorded clinical information during a 14-day enrollment period at each participating site. No study-specific interventions, investigations, or alterations to clinical care will occur.

Data collected will include:

Demographic and clinical characteristics. Comorbidities, frailty status, and cognitive status. Surgical urgency and procedure characteristics. Perioperative clinical variables. Planned and actual postoperative care location. Postoperative morbidity and complications. Delirium status. Unplanned ICU admissions. Need for additional surgical procedures. In-hospital outcomes, including mortality.

The primary objective is to assess the complexity and risk profile of older adults presenting for major surgery in Ireland. Secondary objectives include determining the incidence of major perioperative adverse outcomes, evaluating unmet needs in postoperative care provision, and identifying potentially modifiable patient-related, treatment-related, and system-related factors associated with adverse outcomes.

Approximately 500 participants will be enrolled across multiple Irish hospitals. Study findings will provide important evidence regarding perioperative care delivery and outcomes in Ireland and may inform future healthcare policy, service planning, resource allocation, and quality improvement initiatives for high-risk surgical patients.

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Conditions studied

  • Outcomes Following Major Surgery in Older Adults

Keywords

  • Older adults
  • Major surgery
  • Perioperative medicine
  • Geriatric surgery
  • Critical care
  • Resource utilization
  • Ireland
03

In context

Lead sponsor

University College Hospital Galway is the lead sponsor of 25 studies on the registry; 2 are open to participants now.

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

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Who can participate

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

Study population

Adults aged 60 years and older undergoing major elective or emergency inpatient surgery at participating hospitals in Ireland during the study recruitment period. Eligible participants will include patients admitted for major surgical procedures requiring postoperative hospital care. Patients undergoing day-case procedures, cardiac surgery, neurosurgery, obstetric procedures, or radiological interventions will be excluded in accordance with the study protocol. Participants will be observed prospectively to assess perioperative risk factors, postoperative complications, healthcare resource utilization, and clinical outcomes.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients ≥60 years
  • Emergency surgery (category I, category II or category III) AND/OR Intermediate to Major elective surgery
  • Patient requires an inpatient postoperative stay.
  • ASA grade 2 - 5 (2E to 5E)

Exclusion criteria

Exclusion Criteria:

  • Patients undergoing planned day-case surgery
  • Patients undergoing cardiac surgery, neurosurgery, or radiological or obstetric procedures.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Target follow-up
7 Days
Patient registry
Yes

Groups and cohorts

  • Older Adults Undergoing Major Surgery

    Adults aged 60 years and older undergoing major elective or emergency inpatient surgery at participating hospitals in Ireland. Participants are observed prospectively during their hospital admission to evaluate perioperative characteristics, postoperative complications, critical care requirements, and clinical outcomes. No study-specific interventions are administered, and all care is provided according to standard clinical practice.

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What researchers measure

Primary outcomes

  1. Major Postoperative Complications

    Incidence of major postoperative complications within 7 days of surgery, defined as a Postoperative Morbidity Survey (POMS) score greater than 1.

    Time frame: Within 7 days of surgery

Secondary outcomes

  1. Major Perioperative Adverse Outcomes by Organ System

    Incidence of major perioperative adverse outcomes categorized by organ system.

    Time frame: Within 7 days of surgery or until hospital discharge, whichever occurs first

  2. All-Cause In-Hospital Mortality

    All-cause in-hospital mortality occurring by Day 7 following surgery or hospital discharge if earlier.

    Time frame: Day 7 after surgery or hospital discharge, whichever occurs first

  3. Unplanned Critical Care Admission

    Need for unplanned admission to an Intensive Care Unit (ICU), High Dependency Unit (HDU), or Post-Anesthesia Care Unit (PACU).

    Time frame: Within 7 days of surgery

  4. Postoperative Delirium

    Incidence of postoperative delirium assessed using the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) or the 4 'A's Test (4AT), depending on the patient's level of care.

    Time frame: Within 7 days of surgery

  5. Time From Decision for Surgery to Induction of Anaesthesia

    Time interval between the clinical decision for urgent or emergency surgery and induction of anaesthesia.

    Time frame: Perioperative period

  6. Unmet Need for Postoperative Critical Care

    Percentage of requests for postoperative ICU, HDU, or PACU care that are not provided.

    Time frame: During the index hospital admission

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Swarbrick CJ; SNAP-3 collaborators; Williams K, Evans B, Blake HA, Poulton T, Nava S, Shah A, Martin P, Partridge JSL, Moppett IK. Postoperative outcomes in older patients living with frailty and multimorbidity in the UK: SNAP-3, a snapshot observational study. Br J Anaesth. 2025 Jul;135(1):166-176. doi: 10.1016/j.bja.2025.04.026. Epub 2025 May 27. PubMed 40425395 ↗
  • Pearse RM, Moreno RP, Bauer P, Pelosi P, Metnitz P, Spies C, Vallet B, Vincent JL, Hoeft A, Rhodes A; European Surgical Outcomes Study (EuSOS) group for the Trials groups of the European Society of Intensive Care Medicine and the European Society of Anaesthesiology. Mortality after surgery in Europe: a 7 day cohort study. Lancet. 2012 Sep 22;380(9847):1059-65. doi: 10.1016/S0140-6736(12)61148-9. PubMed 22998715 ↗
  • International Surgical Outcomes Study group. Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries. Br J Anaesth. 2016 Oct 31;117(5):601-609. doi: 10.1093/bja/aew316. PubMed 27799174 ↗
  • Abbott TEF, Fowler AJ, Dobbs TD, Harrison EM, Gillies MA, Pearse RM. Frequency of surgical treatment and related hospital procedures in the UK: a national ecological study using hospital episode statistics. Br J Anaesth. 2017 Aug 1;119(2):249-257. doi: 10.1093/bja/aex137. PubMed 28854546 ↗
  • Pearse RM, Harrison DA, James P, Watson D, Hinds C, Rhodes A, Grounds RM, Bennett ED. Identification and characterisation of the high-risk surgical population in the United Kingdom. Crit Care. 2006;10(3):R81. doi: 10.1186/cc4928. Epub 2006 Jun 2. PubMed 16749940 ↗

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Feb 2027, 3 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 19, 2026
First posted
Oct 26, 2026
StartEst.
Nov 2, 2026
Primary completionEst.
Feb 28, 2027
CompletionEst.
Dec 31, 2027
Last update
Oct 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 26, 2026
Show all 1 update
  1. Oct 26, 2026
    First appeared on the registry

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 ↗

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Registry details

Key details

Study ID
NCT07895199
Lead sponsor
University College Hospital Galway
Responsible party
John Laffey (Professor, University College Hospital Galway) — Principal investigator
First posted
Oct 26, 2026
Start date
Nov 2, 2026 (estimated)
Primary completion
Feb 28, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Oct 26, 2026

Study contacts

John Laffey
Contact
jlaffey@universityofgalway.ie
+353 91898375

Oversight

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

Not currently enrolling

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

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