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 @ 3:25 AM
Ignite Modification Date:
2025-12-25 @ 3:25 AM
NCT ID:
NCT02957305
Eligibility Criteria:
Inclusion Criteria:
* All patients admitted at the Gynecological emergency Unit at Hospital de Clínicas de Porto Alegre scheduled for uterine evacuation with \<12 weeks of gestation.
Exclusion Criteria:
* patients who do not wish to participate in the project;
* patients with ectopic pregnancy;
* patients with comorbidities (heart failure congestive, chronic obstructive pulmonary disease);
* patients with hypovolemic shock;
* patients with cervical incompetence;
* patients with infected miscarriage/abortion (presence of fever, pus from the cervix, leukocytosis \[\> 14000\]);
* patients with twin pregnancy;
* patients with Marfan syndrome;
* patients allergic to misoprostol;
* patients with coagulopathy;
* patients with opening of cervical internal os (4 mm of dilatation at the time of consultation);
* patients with previous surgery of the cervix (conization);
* patients with concomitant use of IUDs.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT02957305
Study Brief:
Protocol Section:
NCT02957305