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Surgical Evacuation of Abortion Under Ultrasonographic Guide

Not Applicable
Completed
Conditions
Abortion
Interventions
Procedure: Blinded evacuation
Procedure: 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
Inclusion Criteria
  • women with non-viable first trimester intrauterine pregnancy
  • no contraindication to surgical evacuation under general anesthesia
Exclusion Criteria
  • gestational age more than 13 weeks
  • hemodynamically unstable
  • suspicion of an ectopic pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Blinded evacuationBlinded evacuationRing evacuation was performed in the conventional way without use of ultrasound followed by sharp gentle curettage until complete evacuation
Evacuation under ultrasound guidanceEvacuation under ultrasound guidanceRing 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
NameTimeMethod
Measurement of endometrial thickness by ultrasound (mm)1 month
Secondary Outcome Measures
NameTimeMethod
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

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