Foley's Catheter Balloon for Induction of Mid Trimester Abortion in Nulliparous Women With or Without Tension Applied

Assiut University

Status: Completed

Conditions: Induction of Abortion

Treatments: Other: No tension group; Other: Tension group; Other: Foley catheter Balloon

Study type: Interventional

Funder types: Other

Identifiers

NCT02842164

FIOA

Details and patient eligibility

About

Induction of abortion is a hot subject that has complex and emotional controversy. The most common time of abortion is the second trimester which represent about 10-15% of all induced abortions over the world. As well as, two-thirds of all serious abortion-related complications are related to induced second trimester abortion.

There are many causes for induction of abortion in the second trimester such as missed abortion, serious fetal abnormalities such as central nervous system or skeletal malformation and lastly some women do not wish to continue a pregnancy and will often seek out termination of pregnancy.

Termination of second trimester is more risky than the first trimester. So many lines have been emerged to achieve safe and effective method of termination of second trimester.

Pharmacologic management seems to be an appealing method for induction of abortion. The combing between mifepristone and misoprostol is the effective regimen for termination of second trimester abortion with success rate reaching about 97-99% within 24 hours.

However, mifepristone is not available or affordable in many countries worldwide so misoprostol have been used alone but it needs higher total dose with lower effectiveness and higher percentage of side effects rate than the combined regimens.

The optimal method for inducing second trimester nulliparous women with an unfavorable cervix is not known. Several studies in literature have described the effectiveness of Foley's catheter in cervical ripening and improvement of Bishop's score in women with unripe cervices . It may act in addition to its mechanical effect by increasing the release of prostaglandin and/or oxytocin release secondary to localized inflammation.

In practice, the insertion of intra-cervical Foley's catheter balloon is followed by applying tension in trial to shorten the time between the insertion and expulsion of the fetus, however; this tension adds more pain for the pregnant women with higher rate of vaginal bleeding and dissatisfaction.

Gary et al in 2016 concluded that the application of tension did not result in faster delivery times, but did result in faster times to catheter expulsion.

Enrollment: 200 patients

Sex: Female

Ages: 20 to 40 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Singleton second trimester (12-28 weeks) pregnancy.
• Nulliparous woman.
• Bishop score ≤ 6.
• BMI 18-22.5 kg/m2

Exclusion criteria

• Multiple gestations.
• Premature rupture of membranes before induction.
• Pregnancy complicated by antepartum hemorrhage (placenta previa or abruptio placenta).
• Low amniotic fluid volume (< 5cm).
• Scarred uterus including hysterotomy or myomectomy.
• Uterine infection.
• Unexplained bleeding.
• Latex allergy

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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200 participants in 2 patient groups

Foley Catheter Balloon with Tension group

Other group

Description:

a 16 French transcervical Foley catheter balloon will be advanced to or past the internal os and the balloon will be filled. Then catheter will be placed on gentle traction by taping the distal tip to the medial thigh for maximum 24 hours. To maintain gentle traction, periodic repositioning of the distal tip on the thigh will be necessary.

Treatment:

Other: Foley catheter Balloon

Other: Tension group

Foley Catheter Balloon without tension group

Other group

Description:

The Foley catheter balloon will be just supported by simple taping to the thigh.

Treatment:

Other: No tension group

Other: Foley catheter Balloon