Phase 4 N=600 Randomized Double-blind Supportive Care

Patient Satisfaction With Propofol for Out Patient Colonoscopy

Colon Cancer · IBS · Polyps

Bottom Line

View on ClinicalTrials.gov: NCT02937506 ↗

Enrolled (actual)

600

Serious AEs

0.0%

Results posted

Sep 2017

Primary outcome: Primary: Patient Satisfaction — 259; 222; 37; 66 Participants

Study Design & Population

Study type: Interventional
Phase: Phase 4
Interventions: Propofol (Drug); Fentanyl Plus Midazolam (Drug)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Mount Carmel Health System
Primary completion: Mar 2016

Outcome Measures

Outcome	Result	p-value
PRIMARY Patient Satisfaction	259; 222; 37; 66; 4; 12	—

Summary

The primary purpose of this study is to determine if patient satisfaction with propofol is better than with non-propofol anesthesia for outpatient colonoscopies.

Eligibility Criteria

Inclusion Criteria

Patients having an outpatient colonoscopy

Exclusion Criteria

High risk patients (ASA IV & V) who are not candidates for colonoscopy in an outpatient center will be excluded.

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Data sourced from ClinicalTrials.gov (NCT02937506). 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.