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 @ 5:03 PM
Ignite Modification Date:
2025-12-24 @ 5:03 PM
NCT ID:
NCT01197950
Eligibility Criteria:
Inclusion Criteria:
* Admission to the labour ward in spontaneous onset of labour
* Latent or active phase of labour
* Nulliparity
* Singleton pregnancy, cephalic presentation
* Gestation: 37+0 to 41+6 (weeks + days)
* Expressed need for labour pain relief
* Swedish speaking (well enough to understand written and oral instructions)
Exclusion Criteria:
* No pharmacological pain relief within 24 hours prior to inclusion into the study
* Severe preeclampsia
* Treatment with oxytocin at the time point of allocation
* Treatment with anticoagulant
* Pacemaker
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT01197950
Study Brief:
Protocol Section:
NCT01197950