MiMi: A Randomized Trial of Mifepristone and Misoprostol for Treatment of Early Pregnancy Failure

Not Applicable

Terminated

Conditions: Early Pregnancy Failure
Miscarriage
Fetal Demise
Anembryonic Pregnancy

Interventions: Drug: Misoprostol and placebo
Drug: Mifepristone and misoprostol

Registration Number: NCT00468299

Lead Sponsor: Boston University

Brief Summary: The purpose of this study is to compare two combinations of drugs (mifepristone and misoprostol versus placebo and misoprostol) used for medical treatment for early pregnancy failure. We will compare the two combinations of medications to see which combination makes miscarriage happen faster. We hypothesize that there will be no difference in time to complete miscarriage between the two groups.

Detailed Description: The optimal method of treating Early Pregnancy Failure (EPF) is not certain. For many years, surgical management of EPF was the only treatment option. Now there are multiple studies demonstrating the effectiveness of misoprostol for treating EPF. Most of the studies investigating medical treatment of EPF have evaluated efficacy at one week. We have found that many women do not want to wait for one week for an outcome of their medical treatment, and want resolution sooner. This has hampered the widespread utilization of medical therapy in our institution.

We propose a regimen of medical treatment for EPF with expeditious follow-up. We want to demonstrate the relative efficacy of two medication regimens for treatment of EPF by performing a randomized trial. One regimen will be 800μg buccal misoprostol alone and the other regimen will be 200mg mifepristone, orally, in addition to 800μg buccal misoprostol, simultaneously. The primary outcome will be complete abortion rates 24hours after medication administration. We hypothesize that mifepristone will not improve complete abortion rates at 24hrs.

Secondary outcomes include rates of abortion by medical treatment at one week, the indications for surgical intervention, relationship of progesterone levels and type of pregnancy failure to outcomes in the two groups. Another secondary objective is to assess satisfaction with the treatment process at the conclusion of pregnancy termination, and 3 weeks after the beginning of the process.

The majority of studies investigating medical treatment of EPF use vaginal misoprostol, but buccal use is increasing. We will use buccal misoprostol, which is widely used at our institution. We will assess the efficacy of this route of administration as well as assess patient acceptability of this method.

Recruitment & Eligibility

Status: TERMINATED

Sex: Female

Target Recruitment: 16

Inclusion Criteria

Age >18yrs, able to read and write English
Intrauterine gestations with anembryonic sac between 10 and 45mm or
10-15mm sac with no growth in three days or other radiologic signs of abnormal pregnancy such as irregular sac or debris within the gestational sac
An embryonic pole <30mm with no cardiac activity

Exclusion Criteria

Intrauterine gestations with CRL <5mm or >30mm without cardiac activity
Incomplete abortion as defined as open cervix and large amount of cramping/bleeding
Hemodynamic instability and/or heavy vaginal bleeding
Hemoglobin less than or equal to 8
Inability to follow-up (ie, lack of transportation or access to telephone)
Bleeding disorder or taking anticoagulants
Prior medical or surgical treatment of the current pregnancy
Obvious Infection
Active Lactation
Allergy to mifepristone or misoprostol
Chronic corticosteroid use
Severe gastrointestinal disease (e.g inflammatory bowel disease, severe gastritis)

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Misoprostol and placebo	Misoprostol and placebo	Women in this arm receive placebo and misoprostol 800 mcg buccally
Mifepristone and misoprostol	Mifepristone and misoprostol	Womwn in this group receive mifepristone 200 mg orally and misoprostol 800 mcg buccally

Primary Outcome Measures