Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:55 PM
Ignite Modification Date:
2025-12-24 @ 1:55 PM
NCT ID:
NCT06861595
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years
* Patients who are difficult to infuse according to the nurse's subjective assessment after the tourniquet has been applied; this may particularly concern patients who are obese, dark-skinned, multi-drug users, sickle-cell anaemia sufferers, drug addicts, elderly with fragile skin and subcutaneous haematomas
* Patients with a medical prescription for intravenous route
* Patients affiliated to a social security scheme
* For women of childbearing age: effective contraception (oral contraceptives, intra-uterine devices or condoms) or post-menopausal women (no menstrual period for 12 months).
* Patient has read and understood the information letter and signed the consent form
Exclusion Criteria:
* Contraindication to fitting a intravenous route (burns to all four limbs, etc.)
* Extreme urgency to have a intravenous route, incompatible with the study, because of a loss of chance due to loss of time
* Patients unable to consent to participation in research
* Pregnant or breastfeeding women or women in labour
* Person deprived of liberty by administrative or judicial decision or person placed under court protection/guardianship or curatorship
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06861595
Study Brief:
Protocol Section:
NCT06861595