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Misoprostol 400 µg Versus 200 µg for Cervical Ripening in 1st Trimester Miscarriage (MISO200)

H

Hospital de Clinicas de Porto Alegre

Status and phase

Completed
Phase 4

Conditions

Miscarriage in First Trimester

Treatments

Drug: Misoprostol 400mcg Tab
Drug: Misoprostol 200mcg Tab

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Local current protocol for cervical ripening in 1st trimester miscarriage recommends 400 µg of misoprostol intravaginally 3 hours before uterine evacuation. This regime has been recommended by some international guidelines . So far, there are no recent studies comparing cervical dilatation between 400 µg of misoprostol and a reduced dose (e.g., 200 µg) for 6 hours. If cervical ripening is similar between these two regimens(i.e., 200µg regimen is not inferior to 400µg regimen), costs reductions and lower side effects may be issued without losing quality of cervix dilatation.

Full description

Miscarriage is defined by the World Health Organization as the interruption of the pregnancy up to 20-23 weeks, or the products of pregnancy weighing less than 500 grams (1). Nearly 15% of known pregnancies end in miscarriage, especially in the first 12 weeks. Estimates indicate that 68000 women die worldwide each year, as a result of unsafe abortions. Abortions are the major cause of maternal death, particularly in Latin America and the Caribbean. In cases of retained and incomplete abortions, uterine emptying is recommended. In the first trimester of pregnancy, either pharmacological or surgical procedure is accepted according to international guidelines.

Pharmacological treatment for uterine evacuation includes the administration of mifepristone and misoprostol or misoprostol alone. Nevertheless, surgical methods have been shown a greater acceptability and patient satisfaction due to a reduced incidence of adverse effects. Currently, Manual Vacuum Aspiration (MVA) is the technique recommended by the Brazilian Ministry of Health and the Brazilian Federation of Gynecology and Obstetrics.

MVA should be performed after cervical ripening. This pre-surgical procedure makes the procedure safer and more effective. In Brazil, misoprostol is the most suitable drug to be used in these cases because of its efficacy, ease of use, low cost, stability at room temperature, and availability. Misoprostol is a synthetic prostaglandin E1 analog and can be administered by oral, sublingual, buccal, rectal, and vaginal routes.

Enrollment

211 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

211 participants in 2 patient groups

Misoprostol 400 µg
Active Comparator group
Description:
Participants received misoprostol 400 µg: 2 tablets of misoprostol (200µg each) introduced into the vagina, at least 6 hours before the Manual Vacuum Aspiration (MVA) procedure.
Treatment:
Drug: Misoprostol 400mcg Tab
Misoprostol 200 µg
Experimental group
Description:
Participants received misoprostol 200 µg: 1 tablet of misoprostol introduced into the vagina, at least 6 hours before the Manual Vacuum Aspiration procedure.
Treatment:
Drug: Misoprostol 200mcg Tab

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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