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Not Yet RecruitingNCT07445256

Recovery Hypoxemia After Sedated Upper Gastrointestinal Endoscopy

Incidence, Duration, and Clinical Impact of Recovery-Period Hypoxemia Following Sedated Upper Gastrointestinal Endoscopy: A Prospective Observational Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Istinye University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Sedation during upper gastrointestinal endoscopy may lead to respiratory events not only during the procedure but also in the early recovery period. Although most hypoxemic episodes are considered transient, their frequency, duration, and clinical consequences during recovery remain insufficiently defined. This prospective observational study aims to evaluate the incidence, duration, and clinical impact of recovery-period hypoxemia following sedated upper gastrointestinal endoscopy. Hypoxemia is defined as SpO₂ \<90% lasting ≥10 seconds. Associated respiratory events and potential risk factors will be analyzed without altering routine clinical practice.

Conditions

Interventions

TypeNameDescription
OTHERSedated Upper Gastrointestinal EndoscopyRoutine upper gastrointestinal endoscopy performed under anesthesiologist-administered sedation. No experimental intervention is applied; the study prospectively observes respiratory events during the recovery period as part of standard clinical care.

Timeline

Start date
2026-02-28
Primary completion
2026-03-15
Completion
2026-03-20
First posted
2026-03-03
Last updated
2026-03-03

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07445256. Inclusion in this directory is not an endorsement.