- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03349853
Description of the Use of Subcutaneous Acetaminophen in Palliative Care Unit in France: Descriptive Questionnaire Survey (EnPasc)
November 21, 2017 updated by: Centre Hospitalier Régional Metz-Thionville
Description of the Use of Subcutaneous Acetaminophen in Palliative Care Unit
Acetaminophen is a drug commonly used in palliative care unit, for its antalgic and antipyretic effects.
Several administration routes are possible but the use of the sub-cutaneous route is actually not supported by recommandations.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
131
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
doctors responsible for palliative care unit in France
Description
Inclusion Criteria:
- doctors responsible for palliative care unit in France
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
knowledge about the use of subcutaneous acetaminophen in palliative care unit.
Time Frame: day 1
|
questionnaire
|
day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 18, 2016
Primary Completion (Actual)
June 18, 2016
Study Completion (Actual)
June 18, 2016
Study Registration Dates
First Submitted
November 17, 2017
First Submitted That Met QC Criteria
November 21, 2017
First Posted (Actual)
November 22, 2017
Study Record Updates
Last Update Posted (Actual)
November 22, 2017
Last Update Submitted That Met QC Criteria
November 21, 2017
Last Verified
November 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 2016-04Obs-CHRMT
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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