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Foley Balloon for Cervical Preparation Before Dilation and Evacuation

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Stony Brook University

Status

Enrolling

Conditions

Abortion, Second Trimester
Abortion, Medical

Treatments

Device: Foley Balloon Catheter
Device: Laminaria
Drug: Misoprostol

Study type

Interventional

Funder types

Other

Identifiers

NCT06850974
IRB2023-00297
stony brook university (Other Identifier)

Details and patient eligibility

About

To evaluate the Foley Balloon technique for cervical preparation before second trimester surgical abortion between 16 and 21 weeks estimated gestational age in combination with misoprostol to prepare the cervix before dilation and evacuation (D&E) instead of osmotic dilators (Laminaria).

Specific Aim One: Assess definitively whether using a Foley Balloon and Misoprostol is non-inferior to osmotic dilators for cervical preparation before D&E.

Specific Aim Two: Evaluate patient satisfaction with the two methods of second trimester abortion.

Specific Aim Three: Evaluate provider satisfaction with the two methods of second trimester abortion.

Full description

Termination of pregnancy was legalized in Mozambique in 2016 for any reason until 12 weeks, and up 16 weeks in cases of rape, and at any time for cases of fetal demise, severe fetal anomaly, or to protect a woman's physical or mental health. It is also legal up until 24 weeks in the case of a chronic infectious or degenerative disease. Termination of pregnancy can be accomplished either by induction of labor or by Dilation and Evacuation (D&E). Typically, D&E after 16 weeks is a two-day procedure. The first day is devoted to cervical preparation, where osmotic dilators are placed into the cervix and allowed to slowly soften and dilate the cervix. On the second day of the procedure the uterus is evacuated. Osmotic dilators are expensive and unavailable in most of Sub-Saharan Africa. An alternative strategy to cervical preparation has recently been developed by Dr. Yashica Robinson and has been described in a retrospective cohort study. This new technique involves using a Foley Catheter balloon (FB) inserted into the cervix to dilate the cervix over several hours with buccal misoprostol as an adjunct medication. After which, the procedure is completed using the dilation and evacuation procedure. However, Foley Balloon for cervical preparation before dilation and evacuation is still considered investigational. Both Foley Balloon and misoprostol are low cost and widely available in Africa and thus may be a safe and efficacious alternative to osmotic dilators. These two strategies of cervical preparation have never been directly compared in a prospective randomized clinical trial. This study aims to conduct a randomized controlled trial to evaluate the Foley Balloon for cervical preparation before D&E. Specifically, our objective is to evaluate the Foley Balloon technique for cervical preparation before second trimester surgical abortion between 16 and 21 weeks estimated gestational age. The investigators propose to conduct a randomized controlled non-inferiority trial to compare procedure difficulty, complication rates, provider satisfaction, and patient satisfaction with a novel technique to prove that the Foley Balloon and misoprostol method is safe, effective, and acceptable to providers and patients.

Enrollment

102 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women 18 years and older presenting to Hospital Central de Maputo requiring abortion for any legal indication between 16-21 weeks gestation.
  • Portuguese speaking

Exclusion criteria

  • Less than age 18
  • Incarcerated
  • Chorioamnionitis
  • Active heavy bleeding
  • A known bleeding diathesis
  • Hemodynamic instability
  • > 2 cm dilation
  • History of cervical cerclage
  • Allergy to any study medications
  • Eclampsia
  • Glasgow Coma Score Less than 15

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

102 participants in 2 patient groups

Foley Balloon and misoprostol
Experimental group
Description:
Patients in the Foley Balloon arm will have a Foley balloon catheter placed trans-cervically and also receive misoprostol per protocol
Treatment:
Drug: Misoprostol
Device: Foley Balloon Catheter
Laminaria
Active Comparator group
Description:
Patients in the Laminaria arm will have a Laminaria placed in the cervix and it will be left in situ per protocol
Treatment:
Device: Laminaria

Trial contacts and locations

1

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Central trial contact

Sierra Washington, MD MSc

Data sourced from clinicaltrials.gov

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