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CompletedNCT02514135Updated Aug 27, 2018

Intra-abdominal Hypertension in Critically Ill Patients

An observational study in Intra-Abdominal Hypertension and Abdominal Compartment Syndrome, sponsored by Western University, Canada. Completed at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-08-27.

Sponsored by Western University, Canada · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
286
Ages
18 Years and older
Sex
All
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Study summary

The aim of the proposed study is to determine the incidence and prevalence of intra-abdominal hypertension and abdominal compartment syndrome in consecutive intensive care admissions using broad inclusion criteria.

Read the detailed description

Increased pressure within the abdominal cavity is particularly common in intensive care patients and has been shown to be an independent risk-factor for mortality in this patient population. The quoted rates of intra-abdominal hypertension of range anywhere from 20-60% are dependent on the population of patient studied. The prospective observational studies performed to date have been underpowered, used strict inclusion/exclusion criteria or were performed prior to consensus guidelines on the definition and measurement of intra-abdominal pressure and hypertension.

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Conditions studied

  • Intra-Abdominal Hypertension
  • Abdominal Compartment Syndrome
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In context

Compartment Syndromes

75 studies on the registry are indexed under Compartment Syndromes; 12 are open to participants now.

This study's planned enrollment of 286 is above the median of 110 across 30 observational studies indexed under Compartment Syndromes.

Browse Compartment Syndromes studies →

Lead sponsor

Western University, Canada is the lead sponsor of 221 studies on the registry; 56 are 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
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All adults (>18 years of age) admitted to the intensive care unit at Victoria Hospital, London, Ontario who have a Foley catheter in-situ

Inclusion criteria

  • Foley catheter in-situ on admission

Exclusion criteria

Exclusion Criteria:

  • Contra-indication to bladder pressure measurement
  • Home service asked that patient is not included
  • Death within 24 priors of admission before bladder pressure measured
  • No bladder pressure performed within 24 hours of admission
  • Consent refused or unable to be obtained (lack of SDM, patient unable to provide)
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
286 participants (estimated)
Patient registry
No

Groups and cohorts

  • Elevated Intra-abdominal Pressure

    Patients with intra-abdominal pressure \> 12 mmHg at any time throughout admission

    Other: No intervention

  • Normal Intra-abdominal Pressure

    Patients with intra-abdominal pressure \< 12 mmHg throughout admission

    Other: No intervention

Interventions

  • OtherNo intervention
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What researchers measure

Primary outcomes

  1. Mortality

    As measured prospectively by patient death in the ICU

    Time frame: While patient in-hospital, expected stay one week on average

Secondary outcomes

  1. Length of stay

    Measured prospectively from date of admission to ICU to death, or discharge from ICU

    Time frame: While patient in-hospital, expected stay one week on average

  2. Abdominal decompression

    Midline laparotomy for abdominal compartment syndrome

    Time frame: While patient in-hospital, expected stay one week on average

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Study locations

1 site
  • Victoria Hospital
    London, Ontario N6K 1C2, Canada
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References and documents

Publications

  • Kirkpatrick AW, Roberts DJ, De Waele J, Jaeschke R, Malbrain ML, De Keulenaer B, Duchesne J, Bjorck M, Leppaniemi A, Ejike JC, Sugrue M, Cheatham M, Ivatury R, Ball CG, Reintam Blaser A, Regli A, Balogh ZJ, D'Amours S, Debergh D, Kaplan M, Kimball E, Olvera C; Pediatric Guidelines Sub-Committee for the World Society of the Abdominal Compartment Syndrome. Intra-abdominal hypertension and the abdominal compartment syndrome: updated consensus definitions and clinical practice guidelines from the World Society of the Abdominal Compartment Syndrome. Intensive Care Med. 2013 Jul;39(7):1190-206. doi: 10.1007/s00134-013-2906-z. Epub 2013 May 15. PubMed 23673399 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 27, 2018, 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
NCT02514135
Lead sponsor
Western University, Canada
Responsible party
Patrick Murphy (Resident, Western University, Canada) — Principal investigator
First posted
Aug 3, 2015
Start date
Sep 1, 2015
Primary completion
Jan 30, 2016
Completion
May 30, 2016
Last update
Aug 27, 2018

Study contacts

Kelly N Vogt, MD
principal investigator · Western University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

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