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:
2025-12-25 @ 1:16 AM
Ignite Modification Date:
2025-12-25 @ 1:16 AM
NCT ID:
NCT04056793
Eligibility Criteria:
Inclusion Criteria:
* Informed consent as documented by signature
* Parturient in situation of mechanical dystocia (non engagement at full dilation)
Exclusion Criteria:
* Inability or medical contraindications to undergo the investigated intervention (e.g. orthopaedic injury or disease preventing the parturient from adopting the optimised position)
* Clinically significant concomitant diseases
* Incapacity of judgment
* Inability to follow the procedures of the study due to language problems, psychological disorders, dementia, etc.
* Foetus cardiac rhythm disorder
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT04056793
Study Brief:
Protocol Section:
NCT04056793