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Enrolling by invitationNCT07691710Updated Jul 9, 2026

Arterial Blood Gas Levels, Oxygen Saturation, and Pressure Injury Risk in ICU Patients

An observational study in Pressure Injury and Intensive Care Unit (ICU), sponsored by Istanbul University. Enrolling by invitation at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Istanbul University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
122
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to examine the relationship between arterial blood gas (ABG) parameters and oxygen saturation (SpO₂) levels and the risk of pressure injury development in patients hospitalized in intensive care units, and to provide a scientific contribution to the processes for assessing pressure injury risk based on the findings obtained.

Read the detailed description

Pressure injuries are defined as localized damage to the skin and/or underlying soft tissue caused by prolonged pressure and/or shear forces, and they most commonly occur over bony prominences (Han et al., 2025). In intensive care patients, these injuries lead to serious consequences such as pain, risk of infection, prolonged hospital stay, and mortality (Labeau et al., 2021). In critically ill patients, inadequate tissue perfusion and oxygenation are identified as one of the main pathophysiological mechanisms involved in the development of pressure injuries (Han et al., 2025). Hypoxia, which occurs when cells are unable to meet their metabolic needs, reduces tissue tolerance and adversely affects the healing process. While insufficient oxygen inhibits collagen synthesis and cellular regeneration, it also reduces blood flow by causing vasoconstriction (Lucchini et al., 2024). This causes tissues in areas exposed to pressure to be more easily damaged.

Therefore, monitoring oxygenation levels is critically important in predicting the risk of pressure injury development. Han et al. (2024) demonstrated that as PaO₂ levels decrease, the risk of pressure injury increases significantly, and that this relationship is supported by a nonlinear dose-response curve. On the other hand, it has been suggested that oxygen saturation may be a more reliable indicator than PaO₂, and that the risk may increase up to sixfold at low oxygen saturation levels (Rahimi-Bashar et al., 2025).

In this context, this study aims to evaluate the relationship between arterial blood gas parameters - pH, PaO₂, PaCO₂, and HCO₃- - and oxygen saturation (SpO₂) levels and the risk of pressure injury development in intensive care patients from the perspective of nursing care.

02

Conditions studied

  • Pressure Injury
  • Intensive Care Unit (ICU)

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03

In context

Pressure Ulcer

545 studies on the registry are indexed under Pressure Ulcer; 129 are open to participants now.

This study's planned enrollment of 122 is below the median of 138 across 110 observational studies indexed under Pressure Ulcer.

Browse Pressure Ulcer studies →

Lead sponsor

Istanbul University is the lead sponsor of 511 studies on the registry; 78 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 1 (20%) have results posted.

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

Patients eligible for inclusion in the study are those aged 18 years and older who have been hospitalized in the intensive care unit for at least 72 hours, are conscious or sedated, and from whom an arterial blood gas sample can be obtained. In addition, patients themselves or their relatives must agree to participate in the study.

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 who have been hospitalized in the intensive care unit for at least 72 hours,
  • Patients aged 18 years and older,
  • Patients who are conscious or sedated and from whom an arterial blood gas sample can be obtained,
  • Patients or their relatives who agree to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Patients with superficial skin lesions or existing pressure injuries, or a history of pressure injuries,
  • Patients whose intensive care unit stay is shorter than 72 hours,
  • Patients diagnosed with diabetes,
  • Patients with circulatory problems.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
122 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • Intensive Care Unit Patients

    Patients admitted to the intensive care unit whose arterial blood gas parameters, including pH, PaO2, PaCO2, and HCO3-, and oxygen saturation levels will be evaluated in relation to the risk of pressure injury development. No intervention will be administered.

06

What researchers measure

Primary outcomes

  1. Risk of Pressure Injury Development

    The risk of pressure injury development in intensive care unit patients will be assessed in relation to arterial blood gas parameters and oxygen saturation levels.

    Time frame: From intensive care unit admission until discharge from the intensive care unit or study completion, up to 12 months.

07

Study locations

1 site
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07691710
Responsible party
Berna Bugan (Research Assistant, Istanbul University) — Principal investigator
First posted
Jul 9, 2026
Start date
Mar 26, 2026
Primary completion
Dec 30, 2026 (estimated)
Completion
Jan 15, 2027 (estimated)
Last update
Jul 9, 2026

Study contacts

Berna Bugan, Research Assistant
principal investigator · Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Oversight

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

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