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 @ 11:53 PM
Ignite Modification Date:
2025-12-24 @ 11:53 PM
NCT ID:
NCT06917651
Eligibility Criteria:
Inclusion Criteria:
* Adult patient
* Patient with a pain rating on the Numerical Rating Scale (NRS) ≥ 4
* Pain of monotraumatic origin in the upper or lower limb
* Glasgow Coma Scale = 15
* SaO2 \> 95% in ambient air
Exclusion Criteria:
* Polytrauma
* Analgesic treatment within the 4 hours preceding admission (except paracetamol)
* Woman of childbearing age without effective contraception, declaring pregnancy or at risk of pregnancy, breastfeeding woman, or positive pregnancy test at inclusion
* Patient requiring intravenous access upon admission (e.g., displaced open fracture)
* Contraindication or allergy to any of the molecules in the analgesia protocol
* Refusal to participate
* Known substance abuse or psychiatric disorders
* Known oxygen dependence or COPD
* Not affiliated with social security
* Patient under guardianship, curatorship, deprived of liberty, or under legal protection
* Patient who does not speak or read French
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06917651
Study Brief:
Protocol Section:
NCT06917651