Exploring the effects of hemp seeds on allergies
Hemp Seed Awareness
NA · University Hospital, Angers · NCT04841954
This study tests whether people with allergies might react to hemp seeds and looks at their nutritional benefits for those with atopic conditions.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 600 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Angers (other gov) |
| Locations | 1 site (Angers) |
| Trial ID | NCT04841954 on ClinicalTrials.gov |
What this trial studies
This study investigates the potential allergic reactions associated with hemp seeds, focusing on their nutritional benefits and the implications of cross-allergy in atopic individuals. Participants will undergo a prick-test to assess their skin reactivity to hemp. The research aims to enhance understanding of hemp's role in allergies, particularly in relation to its lipid-transfer proteins. The study is conducted at the Allergology Unit of the University Hospital of Angers.
Who should consider this trial
Good fit: Ideal candidates include adults referred to the Allergology Unit who can provide informed consent and are affiliated with a social security scheme.
Not a fit: Patients who are pregnant, have severe eczema, or cannot understand French may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into managing allergies related to hemp seeds and improve dietary recommendations for atopic patients.
How similar studies have performed: While there is limited research specifically on hemp seed allergies, studies on cannabis-related allergies have shown varying degrees of success, indicating a need for further exploration in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Major patient * Patient referred to the Allergology Unit of the Hospital of Angers, in consultation or in Hospitalization - for conducting prick-tests * Patient affiliated or beneficiary of a social security scheme * Patient with informed consent Exclusion Criteria: * Pregnant women, parturients * Persons deprived of liberty by administrative or judicial decision * Persons receiving psychiatric care under duress * Adults under legal protection measure * People out of state to express consent * people not able to understand French language * Patients whose skin reactivity prevents interpretation of tests (patients who cannot interrupt anti-histamines or have severe eczema)
Where this trial is running
Angers
- MORISSET Martine — Angers, France (RECRUITING)
Study contacts
- Study coordinator: Martine MORISSET
- Email: martine.morisset@chu-angers.fr
- Phone: 0241353637
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Allergy