Mifepristone and Misoprostol Versus Misoprostol Alone for Missed Abortion: A Randomized-controlled Trial

Gynuity Health Projects

Status and phase: Terminated; Phase 4

Conditions: Missed Abortion; Pregnancy

Treatments: Drug: Misoprostol; Drug: Mifepristone

Study type: Interventional

Funder types: Other

Identifiers

NCT02342002

1015

Details and patient eligibility

About

The purpose of the proposed study is to compare - in a randomized, placebo-controlled, double-blinded trial - a combination of mifepristone and misoprostol to misoprostol used alone for missed abortion.

Full description

The primary aim of this trial is to compare the efficacy of mifepristone-misoprostol versus misoprostol alone for treatment of missed abortion. This will be a randomized controlled double-blinded trial of 416 women comparing misoprostol alone to mifepristone plus misoprostol for treatment of missed abortion less than 13 weeks+ 0 days LMP. All women in the trial will undergo routine screening (including ultrasound) and pre-medical induction care per standard practice at the hospital. All eligible women agreeing to participate in the study will be randomized to receive one of the following regimens: 1) STUDY GROUP ONE: 200mg mifepristone followed in 24 hours by 800mcg sublingual misoprostol; 2) STUDY GROUP TWO: placebo followed in 24 hours by 800mcg sublingual misoprostol.

Enrollment: 416 estimated patients

Sex: Female

Ages: 18 to 49 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Ultrasound examination demonstrating:

  1. Evidence of fetal demise (no fetal cardiac activity despite recognizable embryo and dates consistent with the likelihood of visible pregnancy) OR
  2. Empty gestational sac with no evidence of incomplete abortion or growth over a 7-day period confirmed by two ultrasounds performed one week apart.

• If fetus exists, fetal size less than 12 weeks+6 days

• Closed cervical os

• Eligible to consent for research according to local regulations

Exclusion criteria

• Active bleeding at enrollment and/or history of bleeding within the prior week
• Allergies or other contraindications to the use of mifepristone or misoprostol
• Suspected ectopic pregnancy
• History of trophoblastic disease
• Coagulation disorder and/or currently taking anticoagulants
• Any serious medical condition

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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416 participants in 2 patient groups, including a placebo group

Mifepristone-misoprostol regimen

Experimental group

Description:

After a woman is determined eligible and signs the informed consent document, she will receive 200 mg mifepristone and advised to swallow the pill when they arrive at home. 24 hours after administration of the mifepristone, women will administer the four tablets of 200 mcg misoprostol sublingually.

Treatment:

Drug: Mifepristone

Drug: Misoprostol

Misoprostol alone regimen

Placebo Comparator group

Description:

After a woman is determined eligible and signs the informed consent document, she will receive a placebo (of same shape and size of mifepristone) and advised to swallow the pill when they arrive at home. 24 hours after administration of the mifepristone, women will administer the four tablets of 200 mcg misoprostol sublingually.

Treatment:

Drug: Misoprostol