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Does Capnography Prevent Hypoxemia During Endoscopic Retrograde Cholangiopancreatography and Endoscopic Ultrasound?

Primary Purpose

Hypoxemia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Capnography
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypoxemia focused on measuring Hypoxemia, Capnography, Apnea, Sedation, ERCP, EUS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults age 18 or greater
  • Subjects undergoing elective ERCP and EUS
  • ASA class 1-3
  • Inpatient and outpatient
  • Able to give informed consent

Exclusion Criteria:

  • ASA Class 4 and 5
  • Emergent procedures
  • Procedures requiring MAC sedation
  • Subjects unable to give informed consent
  • Subjects on oxygen before procedure
  • Subjects on CPAP/BiPAP
  • Allergies to fentanyl/demerol/midazolam

Sites / Locations

  • Cleveland Clinic Foundation

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Capnography

Standard Monitoring

Arm Description

Capnography: Subjects randomized to capnography-titration arm: The endoscopy team would be made aware of the capnographic abnormalities as they arise. In this arm, the endoscopy team will have the graphic representation of respiratory activity (capnography) as well as end-epxiratory levels of carbon dioxide in addition to the normal physiologic monitoring portfolio of pulse oximetry, blood pressure and electrocradiography. This observation phase would take place for a baseline prior to sedation, during the administration of sedation as well as throughout the procedure. Monitoring for the study would stop upon completion of the endoscopic procedure.

Subjects randomized to capnography-blinded arm: In this arm, the endoscopy team will not have the graphic representation of respiratory activity (capnography) as well as end-expiratory levels of carbon dioxide available. Only a standard of care physiologic monitoring portfolio of pulse oximetry, blood pressure and electrocradiography at the disposal of the endoscopy team to titrate the sedative medications.

Outcomes

Primary Outcome Measures

Number of Participants Experiencing Hypoxemia During Endoscopy
Hypoxemia was defined as oxygen saturation less than 90 percent for at least 15 seconds.

Secondary Outcome Measures

Proportion of Participants Requiring Supplemental Oxygen
Proportion of Participants Experiencing Severe Hypoxemia
Proportion of Participants Experiencing Apnea

Full Information

First Posted
March 30, 2008
Last Updated
October 24, 2017
Sponsor
The Cleveland Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT00675415
Brief Title
Does Capnography Prevent Hypoxemia During Endoscopic Retrograde Cholangiopancreatography and Endoscopic Ultrasound?
Official Title
Does Capnography Prevent Hypoxemia During ERCP and EUS? A Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Cleveland Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Subjects undergoing elective ERCP and EUS will receive standard monitoring and sedation. In addition, capnography which measures carbon dioxide levels and can graphically assess respiratory activity will be used. Subjects will be randomized to either a capnography blinded or titration arm. In the capnography titration arm, the endoscopy team would be made aware of capnographic abnormalities as they arise throughout the procedure. In the capnography blinded arm, this information will not be available to the endoscopy team and represents standard of care. It is our hypothesis that using capnography can prevent low oxygen levels known as hypoxemia, during these procedures.
Detailed Description
Subjects undergoing elective ERCP and EUS will receive standard monitoring and sedation. In addition, capnography which measures carbon dioxide levels and can graphically assess respiratory activity will be used. Subjects will be randomized to either a capnography blinded or titration arm. In the capnography titration arm, the endoscopy team would be made aware of capnographic abnormalities as they arise throughout the procedure. In the capnography blinded arm, this information will not be available to the endoscopy team and represents standard of care. It is our hypothesis that using capnography can prevent low oxygen levels known as hypoxemia, during these procedures. The primary outcome of our study is the proportion of patients with hypoxemia in the two arms. Review of the literature indicates that the incidence of hypoxemia without supplemental oxygen varies from 30-70%. Our sample size calculation is based on a reduction of the hypoxemia incidence from 40% to 20%. Secondary outcomes will be the proportions of patients with oxygen requirements, major hypoxemia and apnea (lack of respiratory activity via capnography for at least 15 seconds) in the two arms. We will perform a univariable and multivariable analysis to determine the risk factors for apnea.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoxemia
Keywords
Hypoxemia, Capnography, Apnea, Sedation, ERCP, EUS

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
263 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Capnography
Arm Type
Active Comparator
Arm Description
Capnography: Subjects randomized to capnography-titration arm: The endoscopy team would be made aware of the capnographic abnormalities as they arise. In this arm, the endoscopy team will have the graphic representation of respiratory activity (capnography) as well as end-epxiratory levels of carbon dioxide in addition to the normal physiologic monitoring portfolio of pulse oximetry, blood pressure and electrocradiography. This observation phase would take place for a baseline prior to sedation, during the administration of sedation as well as throughout the procedure. Monitoring for the study would stop upon completion of the endoscopic procedure.
Arm Title
Standard Monitoring
Arm Type
No Intervention
Arm Description
Subjects randomized to capnography-blinded arm: In this arm, the endoscopy team will not have the graphic representation of respiratory activity (capnography) as well as end-expiratory levels of carbon dioxide available. Only a standard of care physiologic monitoring portfolio of pulse oximetry, blood pressure and electrocradiography at the disposal of the endoscopy team to titrate the sedative medications.
Intervention Type
Diagnostic Test
Intervention Name(s)
Capnography
Other Intervention Name(s)
Oridion Capnomater and CapnoBiteBloc
Intervention Description
Capnography: Passive measurement of carbon dioxide via a special bite block which allows graphic assessment of the subject's respiratory activity
Primary Outcome Measure Information:
Title
Number of Participants Experiencing Hypoxemia During Endoscopy
Description
Hypoxemia was defined as oxygen saturation less than 90 percent for at least 15 seconds.
Time Frame
Continuously Assessed during a single endoscopic procedure, typically about 2 hours
Secondary Outcome Measure Information:
Title
Proportion of Participants Requiring Supplemental Oxygen
Time Frame
Continuously measured during endoscopy, typically about 2 hours
Title
Proportion of Participants Experiencing Severe Hypoxemia
Time Frame
Continuously measured during endoscopy, typically about 2 hours
Title
Proportion of Participants Experiencing Apnea
Time Frame
Continuously measured during endoscopy, typically about 2 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adults age 18 or greater Subjects undergoing elective ERCP and EUS ASA class 1-3 Inpatient and outpatient Able to give informed consent Exclusion Criteria: ASA Class 4 and 5 Emergent procedures Procedures requiring MAC sedation Subjects unable to give informed consent Subjects on oxygen before procedure Subjects on CPAP/BiPAP Allergies to fentanyl/demerol/midazolam
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John J Vargo, M.D., M.P.H.
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19422079
Citation
Qadeer MA, Vargo JJ, Dumot JA, Lopez R, Trolli PA, Stevens T, Parsi MA, Sanaka MR, Zuccaro G. Capnographic monitoring of respiratory activity improves safety of sedation for endoscopic cholangiopancreatography and ultrasonography. Gastroenterology. 2009 May;136(5):1568-76; quiz 1819-20. doi: 10.1053/j.gastro.2009.02.004.
Results Reference
derived

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Does Capnography Prevent Hypoxemia During Endoscopic Retrograde Cholangiopancreatography and Endoscopic Ultrasound?

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