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NCT03813849 Clinical Trial

Remnants of Conception After Suction Evacuation of Missed Abortion

Miscarriage Clinical Trial

Official title:
Sonographic Detection of Remnants After Surgical Evacuation of Missed Abortion

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03813849
Other study ID # 0409/016
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 10, 2016
Est. completion date March 30, 2020

Study information
Verified date October 2019
Source University of Alexandria
Contact Mervat S Omran, M.D
Phone +2034226106
Email Mervat.Elsedeek@alexmed.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

All women admitted for surgical evacuation of missed abortion after failure of medical treatment from June 2016 underwent transvaginal sonography immediately after completion of the procedure as judged by the operator to ensure absence of remnants.

Description:

Women indicated for surgical evacuation of missed abortion up to 12 weeks were included. Standard surgical evacuation of uterus by suction followed by sharp curettage under general anaesthesia were done for all cases. When the operator judged the procedure as complete, transvaginal sonography was done by dedicated sonographer using portable ultrasound machine in theatre. If remnants were detected the procedure was repeated till the cavity seen empty.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date March 30, 2020
Est. primary completion date January 30, 2020
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

multiparous. have missed abortion up to 12 weeks gestational age by dating. failed medical evacuation. consented for the procedure.

Exclusion Criteria:

suspicion of sepsis. Suspected molar pregnancy. previous evacuation trial. abnormal uterus like fibroids.

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Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Sonographic examination of uterus after surgical evacuation

Locations
Country Name City State
Egypt Shatby maternity university hospital Alexandria

Sponsors (1)
Lead Sponsor Collaborator
University of Alexandria

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary presence remnants of conception transvaginal sonographic detection immediately after the end of the procedure
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