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 @ 11:57 PM
Ignite Modification Date:
2025-12-24 @ 11:57 PM
NCT ID:
NCT02573051
Eligibility Criteria:
Inclusion Criteria:
* Maternal age ≥20years old.
* No vaginal bleeding.
* No dilation of internal os.
* Gestational age: from 8-11weeks.
* Gestational sac with a mean gestational sac diameter (MGD) greater than 25 mm and no yolk sac, or an MGD \>25 mm with no embryo.
Exclusion Criteria:
* Patients with excessive vaginal bleeding (soaking more than a pad per day).
* Patients with dilated cervix.
* Patients with allergy either to misoprostol or isosorbide mononitrate.
* Those who will be insisted on D and C will be excluded from the study.
* Women will be excluded from the study if they are anemic (hemoglobin less than 11 g/dl).
* Hemo-dynamically unstable with signs of pelvic infection and/or sepsis.
* Suffering from a clotting disorder or using anticoagulants.
* Women with uterine pathology such as myomas or malformation.
* Women had previous caesarian section.
* Asthmatic patients.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT02573051
Study Brief:
Protocol Section:
NCT02573051