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NCT ID: NCT00426491 Completed - Pregnancy Clinical Trials

Misoprostol for Non-Viable Pregnancies

Start date: March 1999
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the effectiveness of Misoprostol (Cytotec; GD Searle and Co., Chicago, IL) for the management of non-viable first trimester pregnancies. Specifically, Misoprostol (15-S-15-methyl PGE1) will be compared to a placebo with expectant management in who have documented non-viable gestations. We will examine the following outcome variables: time to resolution, number of patients requiring dilation and curettage, change in hematocrit, cost to the institution, patient satisfaction, and reported side effects.