|
Main
|
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
|
Register:
|
ClinicalTrials.gov |
|
Last refreshed on:
|
19 February 2015 |
|
Main ID: |
NCT02296866 |
|
Date of registration:
|
18/11/2014 |
|
Prospective Registration:
|
No |
|
Primary sponsor: |
|
|
Public title:
|
Assessment of Prokinetic Effects of Erythromycin in Emergency Patients With a Full Stomach
|
|
Scientific title:
|
|
|
Date of first enrolment:
|
September 2014 |
|
Target sample size:
|
28 |
|
Recruitment status: |
Completed |
|
URL:
|
http://clinicaltrials.gov/show/NCT02296866 |
|
Study type:
|
Observational |
|
Study design:
|
Observational Model: Cohort, Time Perspective: Prospective
|
|
Phase:
|
N/A
|
|
|
Countries of recruitment
|
|
France
| | | | | | | |
|
Key inclusion & exclusion criteria
|
Inclusion Criteria:
- Emergency surgery for trauma
- ASA 1 and 2 patients
- Full stomach (antral area > 550 mm²)
- Adult patients
Exclusion Criteria:
- No contraindication to erythromycin
- Extreme emergency surgery (time frame < 90 min between arrival in the service and the
start of the surgery)
- gastroparesis or pathology associated with gastroparesis
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
|
|
Health Condition(s) or Problem(s) studied
|
|
Full Stomach
|
|
Emergency Surgery
|
|
Primary Outcome(s)
|
|
ultrasonographic measurement of antral area
[Time Frame: 30 minutes and immediately before erythromycin infusion, and 30, 60 and 90 min after the start of erythromycin infusion]
|
|
Secondary ID(s)
|
|
2013-A01257-38
|
|
Source(s) of Monetary Support
|
|
Please refer to primary and secondary sponsors
|
|
Results
|
|
Results available:
|
|
|
Date Posted:
|
|
|
Date Completed:
|
|
|
URL:
|
|
|
|