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 @ 2:08 AM
Ignite Modification Date:
2025-12-25 @ 2:08 AM
NCT ID:
NCT02314260
Eligibility Criteria:
Inclusion Criteria:
1. Primigravida Singleton pregnancy with mature fetus at term indicated for termination of pregnancy.
2. Cephalic presentation.
3. Medical indications for termination of pregnancy e.g.: Pre-eclampsia, uncontrolled diabetes at term..e.t.c,
4. Post-term pregnancy.
5. Fetal indication: signs of fetal compromise e.g.: decreased biophysical profile, poor umbilical Doppler indices, diminished liquor.
6. premature rupture of membranes (PROM) not going into spontaneous labor within 24 hours since onset.
7. Intrauterine fetal death (IUFD).
Exclusion Criteria:
1. they had true labor pains or clear onset of labor as diagnosed by cervical changes.
2. Previous uterine surgery (scared uterus).
3. Cephalo-pelvic disproportion.
4. Mal-presentations
5. Severe oligo-hydramnios i.e.: amniotic fluid index Less than 5.
6. Twin pregnancy.
7. Fetal macrosomia. -Growth beyond a specific threshold (weight above 4000g) 8) Placenta previa.
9\) Fetal bradycardia in case of living fetus.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
34 Years
Study:
NCT02314260
Study Brief:
Protocol Section:
NCT02314260