Verification of the Safety of Normal Food Before a Cerebral Arteriography
VIANAC
1 other identifier
observational
677
1 country
1
Brief Summary
Fasting is currently required before elective cerebral angiography, despite numerous arguments against fasting (kidney toxicity, vasovagal reaction, discomfort) and seams unusefull regarding it's main goal : reducing nausea and vomiting. The investigators propose to assess frequency of nausea and vomiting among patients having taken their breakfast at home before day care angiography. The investigators hypothesise that less than 1% of non fasting patients will suffer of vomitint.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2020
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 10, 2020
CompletedFirst Posted
Study publicly available on registry
July 20, 2020
CompletedStudy Start
First participant enrolled
December 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2024
CompletedJuly 17, 2025
July 1, 2025
4 years
July 10, 2020
July 15, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
frequency of vomiting during arteriographic procedure
The investigators check if there is vomiting or not during the examination noted by an electro radiology manipulator. Safety issue : Bronchus inhalation
fifteen minutes
Secondary Outcomes (1)
nausea
fifteen minutes
Eligibility Criteria
Adult patients benefiting from a cerebral arteriography, within the UMCA of the North Laënnec Hospital.
You may qualify if:
- Adult,
- non fasting,
- day care hosptilalisation
You may not qualify if:
- Childs,
- pregnancy,
- parenteral nutrition,
- nausea,
- vomiting before arteriography,
- arteriography under general anesthesia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU de Nantes
Nantes, 44093, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Benjamin Daumas-Duport, ph
Nantes University Hospital
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 10, 2020
First Posted
July 20, 2020
Study Start
December 1, 2020
Primary Completion
December 1, 2024
Study Completion
December 1, 2024
Last Updated
July 17, 2025
Record last verified: 2025-07