Actively Recruiting
Hemp Seed Awareness Allergy Study at University Hospital, Angers
Led by University Hospital, Angers · Updated on 2024-06-11
600
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating allergies related to hemp seed, a product derived from the Cannabis sativa plant that contains high levels of cannabidiol (CBD) but very low levels of tetrahydrocannabinol (THC). Hemp seed allergies are less studied compared to recreational cannabis allergies, though hemp seeds can cause severe allergic reactions such as anaphylaxis, especially in individuals previously sensitized through skin or respiratory exposure to cannabis. This study aims to better understand the allergenic potential of hemp seeds in people referred to the Allergology Unit. The study involves performing a diagnostic prick-test using hemp seed and flower extracts to detect allergic reactions. Participants will undergo this prick-test on Day 1 to assess skin reactivity to hemp. The study also collects information about participants' history of hemp use to explore possible sensitization routes. No drug or treatment is given as this is an interventional diagnostic study. Participants will be adults referred for allergy testing at the Hospital of Angers, who will have the prick-test performed and their medical and exposure history recorded. Researchers will monitor the results of the prick-test and document any signs of allergy. The primary measure is a positive prick-test response on the first day. The study focuses on safety and accurate allergy identification, with participation involving a single visit for allergy testing and history taking.
CONDITIONS
Brief Title
Hemp Seed Awareness
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years or older
- Referred to the Allergology Unit of the Hospital of Angers for consultation or hospitalization for prick-tests
- Affiliated or beneficiary of a social security scheme
- Provided informed consent
You will not qualify if you...
- Pregnant women or women who have recently given birth
- Persons deprived of liberty by administrative or judicial decision
- Persons receiving psychiatric care under duress
- Adults under legal protection measures
- Persons unable to provide consent
- Persons unable to understand French
- Patients with skin conditions preventing test interpretation (unable to stop antihistamines or severe eczema)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo a hemp seed and flower prick-test to assess allergic response.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
MORISSET Martine
Angers, France
Actively Recruiting
Research Team
M
Martine MORISSET
D
DRCI Promotion Interne
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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