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
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Locations near you
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Full eligibility criteria for NCT01597726
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Woman seeking TOP between 13 and 20 weeks gestation as determined by ultrasound
Age 18 or greater
Willingness to participate in randomized study
Fluency in English, Afrikaans or Xhosa
Ability to give informed consent
Staying within one hour travel time of Tygerberg Hospital for the night prior to the D&E
Ability to be contacted by telephone
Fetal demise confirmed by ultrasound examination
History of bleeding disorder or current anticoagulation therapy
Allergy to misoprostol
Currently breastfeeding and unwilling or unable to temporarily discard milk
More than one prior cesarean delivery
All locations for NCT01597726
South Africa (1)
Cape Town, South Africa, 7505
View full eligibility
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
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