Comparison of effectiveness of placental blood drainage after spontaneous vaginal delivery in
decreasing the duration, blood loss,and complications of the third stage, against no drainage
of placental blood.
Procedure: Placental Blood Drainage
Procedure: not Placental Blood Drainage
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Full eligibility criteria for NCT03020355
Ages eligible for Study
15 Years to 50 Years
Genders eligible for Study
Accepts Healthy Volunteers
Gestational age of 37 weeks (or) more
No major medical (or) obstetric complications
Spontaneous vaginal delivery
History of APH
Large baby (more than 3.5 kg)
Known coagulations disorders
Previous surgeries on the uterus
All locations for NCT03020355
View full eligibility
Tris trial is registered with FDA with number: NCT03020355. The sponsor of the trial is Zeynep Kamil Maternity and Pediatric Research and Training Hospital and it is looking for 200 volunteers for the current phase.
Official trial title: Comparison of Blood Loss in Using vs Not Using Placental Cord Drainage After Spontaneous Vaginal Delivery
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