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 @ 4:14 AM
Ignite Modification Date:
2025-12-25 @ 4:14 AM
NCT ID:
NCT00190320
Eligibility Criteria:
Inclusion Criteria:
* Agreed women Sonographic estimation of begin of pregnancy \<20GW Single pregnancy in cephalic presentation Macrosomic fetus :
* clinical estimation : 36GW : ≥3350g or 34cm 37GW : ≥3550gor34cm 38GW : ≥3750g or 35cm
* sonographic estimation : 36GW : ≥ 3500g 37GW : ≥ 3700g 38GW : ≥ 3900g
Exclusion Criteria:
* Typical diabetes I or typifies II or diabetes gestational treated by insulin.
* Antecedents of tear of the anal sphincter or severe urinary or faecal presence of an incontinence.
* Antecedent of dystocia of the shoulders or neonatal traumatism.
* Antecedents of caesarian or uterine scar.
* contraindication in the release of the work or in the childbirth by low way.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
48 Years
Study:
NCT00190320
Study Brief:
Protocol Section:
NCT00190320