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Patient Satisfaction With Propofol for Out Patient Colonoscopy

NCT02937506 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2017-12-26

Study results available
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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.

Conditions

Interventions

DRUG

Propofol

The intervention is to use propofol as anesthesia during a colonoscopy.

DRUG

Fentanyl Plus Midazolam

The control is to use standard of care anesthesia, fentanyl and midazolam, during a colonoscopy.

Sponsors & Collaborators

  • Mount Carmel Health System

    lead OTHER

Principal Investigators

  • Anantha Padmanabhan, MD · Mount Carmel Health System

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2016-03-31
Completion
2016-08-31

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02937506 on ClinicalTrials.gov