N/A N=452 Randomized Double-blind Other

Use of Capnography in EGD and Colonoscopy With Moderate Sedation.

Hypoxia · Apnea · Hypotension · Hypopnea

Bottom Line

View on ClinicalTrials.gov: NCT01994785 ↗

Enrolled (actual)

452

Serious AEs

0.0%

Results posted

Jul 2017

Primary outcome: Primary: Number of Participants Experiencing Hypoxia During Capnography Monitoring. — 54; 59; 61; 63 Participants

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Capnographic Monitoring (Diagnostic_test)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: The Cleveland Clinic
Primary completion: Feb 2015

Outcome Measures

Outcome	Result	p-value
PRIMARY Number of Participants Experiencing Hypoxia During Capnography Monitoring.	54; 59; 61; 63	—

Summary

This study will provide capnography monitoring during routine upper endoscopy and colonoscopy with moderate sedation in order to see if it improves safety.

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

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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.