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More info
You can access this
clinical trial
if you have
Abortion, Induced
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

The purpose of this study is to compare the efficacy of buccal misoprostol cervical priming to laminaria priming among women undergoing D&E at 13-20 weeks gestation in the Western Cape Province, South Africa

Provided treatments

  • Drug: Misoprostol
  • Device: Laminaria

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01597726. The sponsor of the trial is Ibis Reproductive Health and it is looking for 159 volunteers for the current phase.
Official trial title:
Cervical Priming Before Dilation & Evacuation: a Randomized Controlled Trial