Comparison of efficacy of rectal misoprostol for reduction amount of blood loss in women
undergoing myomectomy, both open and laparoscopic approach
Drug: Rectal Misoprostol
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Full eligibility criteria for NCT02908295
Ages eligible for Study
25 Years to 50 Years
Genders eligible for Study
Accepts Healthy Volunteers
Patient provisionally diagnosed with leiomyoma of uterus with less than 10 cm diameter
Patient undergoing myomectomy, both open and laparoscopic approach
Patient aged 25 - 50 years
Patient able to give free and informed consent and who agrees to participate bu signing the consent form
Patient able to speak and understand Thai
Patient able to complete the questionnaire
Patient who was pathologically diagnosed apart from leiomyoma
Patient with leiomyoma FIGO type 0
Patient who has medical conditions that increase bleeding tendency, such as thrombocytopenia, coagulopathy, renal insufficiency, uncontrolled diabetes mellitus, taking antiplatelets or anticoagulants less than 7 days prior the surgery
Patient who takes prostaglandin analogs and/or antagonists (NSAIDS) less than 7 days prior the surgery.
Patient who may take higher risks of misoprostol adverse effect such as hypertension, ischemic heart disease, glaucoma, asthma
Patient who had and allergic reaction to misoprostol or vitamin B6
All locations for NCT02908295
View full eligibility
Tris trial is registered with FDA with number: NCT02908295. The sponsor of the trial is Rajavithi Hospital and it is looking for 20 volunteers for the current phase.
Official trial title:
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