- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07166718
- Original Trial
Running Title: Correlation Between Pulse Oximeter (SpO2) and ABG (SaO2)
September 2, 2025 updated by: Sumit Shahi, Tribhuvan University Teaching Hospital, Institute Of Medicine.
Correlation of Pulse Oximetry With Arterial Blood Gas Derived Oxygen Saturation in ICU Patients on Supplemental Oxygen - A Prospective Cross-sectional Study
This was a prospective cross-sectional observational study conducted among 152 patients, admitted to Medical Intensive Care Unit (MICU), who required supplemental oxygen during hospital stay.
The ABG analysis was done, and pulse oximeter reading was recorded simultaneously.
The goal of the study was to correlate oxygen saturation measured by pulse oximeter (SpO2) with arterial blood gas analysis (SaO2).
Study Overview
Study Type
Observational
Enrollment (Actual)
152
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Lalitpur, Nepal, 09771
- Sumit Shahi
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All patients admitted in MICU of Chitwan medical college, Chitwan requiring supplemental oxygen.
Description
Inclusion Criteria:
- All patients admitted in MICU requiring supplemental oxygen
Exclusion Criteria:
- Patients party not giving consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hypoxemia
Time Frame: 3 months
|
Correlation between hypoxemia and hypoxia
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2025
Primary Completion (Actual)
July 31, 2025
Study Completion (Actual)
August 30, 2025
Study Registration Dates
First Submitted
September 2, 2025
First Submitted That Met QC Criteria
September 2, 2025
First Posted (Estimated)
September 10, 2025
Study Record Updates
Last Update Posted (Estimated)
September 10, 2025
Last Update Submitted That Met QC Criteria
September 2, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BPandey23
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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