N/A
Completed N=452
Use of Capnography in EGD and Colonoscopy With Moderate Sedation.
Source: ClinicalTrials.gov NCT01994785 ↗Enrolled (actual)
452
Serious AEs
0.0%
Results posted
Jul 2017
Primary outcomePrimary: Number of Participants Experiencing Hypoxia During Capnography Monitoring. — 54; 59; 61; 63 Participants
Summary
This study will provide capnography monitoring during routine upper endoscopy and colonoscopy with moderate sedation in order to see if it improves safety.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Experiencing Hypoxia During Capnography Monitoring. |
54; 59; 61; 63 | — |
Eligibility Criteria
Inclusion Criteria
- >18yrs with full decision making capacity
- Scheduled for elective upper endoscopy or colonoscopy with moderate sedation
Exclusion Criteria
- ASAPS class III or higher.
- History of a demonstrated allergy or intolerance to a benzodiazepine or opioid
- Patients scheduled for both upper endoscopy and colonoscopy during the same endoscopy day
Data sourced from ClinicalTrials.gov (NCT01994785). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.