New monitor may spot breathing trouble in COPD patients during routine procedures
NCT ID NCT07262905
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study observed 100 people with COPD who were sedated for a stomach and colon exam. Researchers wanted to see if certain risk factors, like symptom severity or past hospital stays, could predict breathing problems during the procedure. They also tested a new monitor called the Integrated Pulmonary Index (IPI) to see if it could spot trouble earlier than standard monitors. The study did not test any new treatments, only observed what happened during routine care.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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100 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Jul 2025
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients (≥18 years) with confirmed COPD undergoing elective gastrointestinal endoscopic procedures under sedation analgesia at a tertiary training and research hospital.
- Ages
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18 years and older
- 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 Diagnosed with Chronic Obstructive Pulmonary Disease (COPD) according to GOLD 2024 criteria Classified as ASA physical status I-IV Undergoing elective gastrointestinal endoscopic procedure under sedation analgesia Suitable for sedation outside the operating room Provided written informed consent - Exclusion Criteria: Age \< 18 years Unstable cardiovascular or respiratory condition Requirement for general anesthesia or advanced airway management Pregnancy Known hypersensitivity to sedative medications Refusal or inability to provide informed consent \-
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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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Bursa Yüksek İhtisas Training and Research Hospital
Bursa, Marmara Region, 16310, Turkey (Türkiye)
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