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 @ 4:19 AM
Ignite Modification Date:
2025-12-25 @ 4:19 AM
NCT ID:
NCT03823820
Eligibility Criteria:
Inclusion Criteria: pregnant women at age of 16 or over with a viable pregnancy and who will fulfil the following:
* Group I: Women attending for elective CS.
* Group II: Women admitted for induction of labour and expected to stay stay in hospital for more than 24 hours.
* Group III: Maternal condition that could have direct impact on body fluid including:
1. Pre-eclampsia requiring hospital admission.
2. Hyperemesis gravidarum requiring hospital admission.
3. Major postpartum haemorrhage (equal or greater than 1000 ml following delivery).
* Group IV: gestational age matched controls.
Exclusion criteria:
* Maternal age less than 16 years at booking.
* Women who are not capable of giving consent.
* Women with learning disabilities/difficulties.
* Unable to speak or read English to the appropriate level.
* Prisoners.
* Any others deemed to belong to a vulnerable group.
* Women who require pace maker or defibrillators.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
16 Years
Study:
NCT03823820
Study Brief:
Protocol Section:
NCT03823820