Other Abortion Clinical Trial
Official title:
Comparison Between Sublingual Misoprostol vs. Sublingual Misoprostol and Laminaria For Second Trimester Termination of Pregnancy
1. Comparison between the duration of time from the beginning of cervical preparation
until abortion, between sublingual misoprostol and the combination of sublingual
misoprostol with laminaria for second trimester medical termination of pregnancy (TOP).
2. Comparison between the adverse event rate following Sublingual misoprostol only vs.
Sublingual misoprostol and laminaria given for pregnancy termination.
3. Comparison between the levels of satisfaction rate of women who underwent pregnancy
termination with sublingual misoprostol vs. sublingual misoprostol with laminaria.
A prospective randomized control trial; 50 women undergoing pregnancy termination in the
second trimester (14-28 weeks)in each group.
Following receiving an ethical approval by the local institutional review board (IRB),
committee, consecutively all women in between 14 weeks to 28 weeks; that have a reason for
termination of pregnancy like: intrauterine fetal death or medical or genetic indications
for termination of pregnancy or socioeconomic termination of pregnancy will be offered to
take part in the study. If eligible according to the inclusion and exclusion criteria, women
will be asked to sign a consent form.
All participants will undergo blood exams (CBC, Prothrombin time, Partial thromboplastin
time , and BLOOD TYPING) and ultrasound exam for Confirmation of diagnosis as routinely
indicated for missed abortion at our department
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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Phase 2 | |
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N/A |