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 @ 6:31 PM
Ignite Modification Date:
2025-12-24 @ 6:31 PM
NCT ID:
NCT06502457
Eligibility Criteria:
Inclusion Criteria:
* Parturient over 18
* Parturient who speaks and understands French
* Parturient hospitalised prior to labour
* Membranes intact or ruptured
* Spontaneous or induced labour
* Parturient in latency phase
* Term ≥ 37SA
* END \> 3
* Parturient requiring active pain management (medicinal or non-medicinal)
* Low-risk pregnancy
Exclusion Criteria:
* Parturient under legal protection
* Parturient with a hearing impairment
* Parturient with visual impairment
* Parturient with epilepsy
* Parturient with psychiatric problems
* Pathological pregnancy
* Parturient with chronic pain
* Parturient with addiction-related disorders
* Parturient allergic to paracetamol
* Parturient allergic to phloroglucinol
* Parturient allergic to codeine
* Parturient allergic to nalbuphine
* Parturient allergic to orozamudol
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06502457
Study Brief:
Protocol Section:
NCT06502457