NCT01371903

Brief Summary

Emergency department patients receiving opioid pain medicine such as morphine, fentanyl or Dilaudid are eligible. After medication exhaled carbon dioxide is measured. and recorded.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
278

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2010

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2010

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

June 10, 2011

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 13, 2011

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2012

Completed
Last Updated

March 24, 2014

Status Verified

June 1, 2011

Enrollment Period

2.3 years

First QC Date

June 10, 2011

Last Update Submit

March 20, 2014

Conditions

Keywords

morphinefentanyldilaudidopioidcapnography

Outcome Measures

Primary Outcomes (1)

  • end tidal carbon dioxide

    measured through small nasal cannula (plastic tube at base of nares)

    study start, 30 minutes, 60 minutes, 90 minutes, 120 minutes

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients receiving opioid such as morphine, fentanyl, or dilaudid during their emergency department visit.

You may qualify if:

  • non intubated patients receiving intravenous opioid medications

You may not qualify if:

  • mechanically ventilated patients
  • patients with physiologic shock

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Albany Medical Center Emergency Department

Albany, New York, 12208, United States

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor Emergency Medicine

Study Record Dates

First Submitted

June 10, 2011

First Posted

June 13, 2011

Study Start

August 1, 2010

Primary Completion

November 1, 2012

Study Completion

November 1, 2012

Last Updated

March 24, 2014

Record last verified: 2011-06

Locations