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Non-anesthesiologist Administered Propofol Sedation for Colonoscopy - a Randomized Clinical Trial

Primary Purpose

Digestive System Diseases, Colonoscopy Sedation

Status
Completed
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Non-anesthesiologist propofol sedation
Propofol sedation administered by an anesthesiologist
Colonoscopy
Sponsored by
Hospital Beatriz Ângelo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Digestive System Diseases focused on measuring Colonoscopy, Sedation, Propofol, Non-anesthesiologist propofol administration

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Referred for elective colonoscopy as outpatients
  • Must be able to provide the informed consent

Exclusion Criteria:

  • American Society of Anaesthesiologists (ASA) class >2
  • Pregnant women
  • Difficult airway predictors (more than 2 ou Mallampati >3)
  • Allergy to propofol or its' components
  • IV drugs abuse

Sites / Locations

  • Hospital Beatriz Ângelo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Non-anesthesiologist propofol sedation

Anesthesiologist administered propofol

Arm Description

Bolus propofol sedation by non-anesthesiologist

Propofol sedation administered by an anesthesiologist

Outcomes

Primary Outcome Measures

Minor adverse events
Minor adverse events as defined by the International Sedation Task Force, including peripheral O2 saturation between 75-90% for less than 60 seconds, apnea, airway obstruction, sedation failure, allergic reaction without anaphylaxis, convulsion, brady/tachycardia and hypo/hypertension (>25% change from baseline)

Secondary Outcome Measures

Propofol dosage
Total propofol dosage
Patient satisfaction
A 10 point visual scale on pain
colonoscopy quality indicators
Colonoscopy quality indicators: time to cecum, withdrawal time, adenoma detection rate
Patient satisfaction 2
A 5 point likert scale on patient satisfaction with the sedation

Full Information

First Posted
February 16, 2014
Last Updated
October 8, 2015
Sponsor
Hospital Beatriz Ângelo
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1. Study Identification

Unique Protocol Identification Number
NCT02067065
Brief Title
Non-anesthesiologist Administered Propofol Sedation for Colonoscopy - a Randomized Clinical Trial
Official Title
Non-anesthesiologist Administered Propofol Sedation for Colonoscopy - a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Beatriz Ângelo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Propofol is the preferred sedation for colonoscopy. There is debate on the safety of the administration of propofol by non-anesthesiologists, despite moderate quality evidence that support its' use. There is only one small trial of a direct comparison of propofol sedation by anesthesiologists versus non-anesthesiologists. Our aim is to compare the incidence of sedation related adverse events, the procedural quality indicators, times (onset, recovery, discharge) and patient satisfaction between non-anesthesiologist administered propofol sedation (NAAP) sedation and anesthesiologist propofol sedation. A randomized clinical trial with the incidence of sedation related minor adverse events as primary endpoint will be conducted. Secondary endpoints include procedure quality indicators, propofol dosage and patient satisfaction. A sample size of 330 subjects (2 arms of 165 patients) will be needed in order to obtain 90% power and a 5% significance level to exclude a 15% difference (15 - 30%) in adverse events incidence, estimated from our pilot experience. The sample size was adjusted for a 2% cross-over rate. Informed and consenting patients undergoing colonoscopy examinations will be randomly assigned to one of two arms. One group will be sedated by an anesthesiologist according to a protocol of propofol mono-sedation. The other group will be sedated with propofol boluses, according to the European Society of Gastrointestinal Endoscopy (ESGE) NAAP guideline, with a 3-man team consisting of one endoscopist, one endoscopy nurse and a sedation nurse, trained in NAAP and exclusively dedicated to sedation and patient monitoring.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Digestive System Diseases, Colonoscopy Sedation
Keywords
Colonoscopy, Sedation, Propofol, Non-anesthesiologist propofol administration

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
277 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Non-anesthesiologist propofol sedation
Arm Type
Experimental
Arm Description
Bolus propofol sedation by non-anesthesiologist
Arm Title
Anesthesiologist administered propofol
Arm Type
Active Comparator
Arm Description
Propofol sedation administered by an anesthesiologist
Intervention Type
Drug
Intervention Name(s)
Non-anesthesiologist propofol sedation
Intervention Description
Bolus propofol sedation administered according to non-anesthesiologist propofol sedation guidelines of the European Society of Gastrointestinal Endoscopy
Intervention Type
Drug
Intervention Name(s)
Propofol sedation administered by an anesthesiologist
Intervention Description
Propofol sedation by an anesthesiologist
Intervention Type
Procedure
Intervention Name(s)
Colonoscopy
Intervention Description
Elective total colonoscopy with or without biopsies, polypectomies or mucosal resection, as clinically indicated
Primary Outcome Measure Information:
Title
Minor adverse events
Description
Minor adverse events as defined by the International Sedation Task Force, including peripheral O2 saturation between 75-90% for less than 60 seconds, apnea, airway obstruction, sedation failure, allergic reaction without anaphylaxis, convulsion, brady/tachycardia and hypo/hypertension (>25% change from baseline)
Time Frame
During the sedation period
Secondary Outcome Measure Information:
Title
Propofol dosage
Description
Total propofol dosage
Time Frame
During the colonoscopy - an estimated mean time of 20 minutes
Title
Patient satisfaction
Description
A 10 point visual scale on pain
Time Frame
Before discharge - estimated mean recovery time of 1 hour
Title
colonoscopy quality indicators
Description
Colonoscopy quality indicators: time to cecum, withdrawal time, adenoma detection rate
Time Frame
During the procedure
Title
Patient satisfaction 2
Description
A 5 point likert scale on patient satisfaction with the sedation
Time Frame
Before discharge - estimated mean recovery time of 1 hour

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Referred for elective colonoscopy as outpatients Must be able to provide the informed consent Exclusion Criteria: American Society of Anaesthesiologists (ASA) class >2 Pregnant women Difficult airway predictors (more than 2 ou Mallampati >3) Allergy to propofol or its' components IV drugs abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandre O Ferreira, MD
Organizational Affiliation
Hospital Beatriz Ângelo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Beatriz Ângelo
City
Loures
ZIP/Postal Code
2674-514
Country
Portugal

12. IPD Sharing Statement

Citations:
PubMed Identifier
21072716
Citation
Dumonceau JM, Riphaus A, Aparicio JR, Beilenhoff U, Knape JT, Ortmann M, Paspatis G, Ponsioen CY, Racz I, Schreiber F, Vilmann P, Wehrmann T, Wientjes C, Walder B; NAAP Task Force Members. European Society of Gastrointestinal Endoscopy, European Society of Gastroenterology and Endoscopy Nurses and Associates, and the European Society of Anaesthesiology Guideline: Non-anesthesiologist administration of propofol for GI endoscopy. Endoscopy. 2010 Nov;42(11):960-74. doi: 10.1055/s-0030-1255728. Epub 2010 Nov 11.
Results Reference
background
PubMed Identifier
23702777
Citation
Dumonceau JM, Riphaus A, Beilenhoff U, Vilmann P, Hornslet P, Aparicio JR, Dinis-Ribeiro M, Giostra E, Ortmann M, Knape JT, Ladas S, Paspatis G, Ponsioen CY, Racz I, Wehrmann T, Walder B. European curriculum for sedation training in gastrointestinal endoscopy: position statement of the European Society of Gastrointestinal Endoscopy (ESGE) and European Society of Gastroenterology and Endoscopy Nurses and Associates (ESGENA). Endoscopy. 2013 Jun;45(6):496-504. doi: 10.1055/s-0033-1344142. Epub 2013 May 23. No abstract available.
Results Reference
background
PubMed Identifier
27100716
Citation
Ferreira AO, Torres J, Barjas E, Nunes J, Gloria L, Ferreira R, Rocha M, Pereira S, Dias S, Santos AA, Cravo M. Non-anesthesiologist administration of propofol sedation for colonoscopy is safe in low risk patients: results of a noninferiority randomized controlled trial. Endoscopy. 2016 Aug;48(8):747-53. doi: 10.1055/s-0042-105560. Epub 2016 Apr 21.
Results Reference
derived

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Non-anesthesiologist Administered Propofol Sedation for Colonoscopy - a Randomized Clinical Trial

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