New oxygen method may prevent dangerous drops during gut procedure
NCT ID NCT07493811
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether giving a special high-flow oxygen through the nose during a sedated gut procedure (ERCP) could prevent dangerously low oxygen levels better than standard oxygen. One hundred adults and older patients took part. The goal was to see which method keeps oxygen levels safer and reduces complications like low blood pressure.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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100 people
The number who actually took part.
- Started
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Apr 2025
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥18 years * Patients scheduled for elective endoscopic retrograde cholangiopancreatography (ERCP) * Planned sedation with monitored anesthesia care * ASA physical status I-III * Ability to provide written informed consent * Adult group: 18-64 years * Geriatric group: ≥65 years Exclusion Criteria: * Severe cardiac, pulmonary, renal, neurological, or hepatic disease * Baseline hypotension (systolic arterial pressure \<90 mmHg) or uncontrolled hypertension (systolic arterial pressure \>170 mmHg, diastolic pressure \>100 mmHg) * Pre-existing hypoxaemia (SpO₂ \<90%) * Known hypersensitivity to study medications or a history of sedation-related adverse events * Use of sedative medication within 24 hours prior to the procedure * Refusal to participate
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Namigar Turgut
Istanbul, Turkey (Türkiye)
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Prof.Dr.Cemil Taşcıoğlu City Hospital
Beşiktaş, İ̇stanbul, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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