Surgical Evacuation of Abortion Under Ultrasonographic Guide
- Conditions
- Abortion
- Interventions
- Procedure: Blinded evacuationProcedure: Evacuation under ultrasound guidance
- Registration Number
- NCT02580175
- Lead Sponsor
- Assiut University
- Brief Summary
Abortion is considered the most common cause of fetal demise all over the world. The majority of cases occur in the first trimester. The termination of abortion may be by medical or surgical methods, however; the surgical methods represent the greater part of termination. Therefore, the safety of this procedure is a worldwide public health concern. Many clinical studies have reported the safety of surgical evacuation in the first trimester.
The suction-aspiration or vacuum aspiration is the most common surgical method of induced abortion. This consists of removing the fetus, embryo, placenta, and membranes by suction using a manual syringe or electric pump. However; these techniques always need cervical dilation before aspiration. The menstrual extraction does not require cervical dilation and can be used in very early pregnancy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 200
- women with non-viable first trimester intrauterine pregnancy
- no contraindication to surgical evacuation under general anesthesia
- gestational age more than 13 weeks
- hemodynamically unstable
- suspicion of an ectopic pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Blinded evacuation Blinded evacuation Ring evacuation was performed in the conventional way without use of ultrasound followed by sharp gentle curettage until complete evacuation Evacuation under ultrasound guidance Evacuation under ultrasound guidance Ring evacuation was performed under ultrasound guidance followed by sharp gentle curettage until complete evacuation. The surgery was considered complete when the endometrial cavity appeared as a regular echogenic line.
- Primary Outcome Measures
Name Time Method Measurement of endometrial thickness by ultrasound (mm) 1 month
- Secondary Outcome Measures
Name Time Method Measurement of blood loss (mL) 1 month measurement of operative time (minutes) 1 month measurement of Hemoglobin level(g/ml) 1 month
Trial Locations
- Locations (1)
Women Health Hospital - Assiut university
🇪🇬Assiut, Egypt