Use of Fetoscopy in Missed Abortion

Abortion, Missed Clinical Trial

Official title:

Use of Fetoscopy in Missed Abortion

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03799081
• Other study ID #: HYMC-00056-18
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 2019
• Est. completion date: January 2021

Study information

• Verified date: January 2019
• Source: Hillel Yaffe Medical Center
• Contact: Emiliya Ilizirov, MD
• Phone: 972-532323246
• Email: emiliyailizirova[@]gmal.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the use of hysteroscopic embryoscopy or fetoscopy as a powerful diagnostic tool to provide better counseling for couples having experienced pregnancy loss.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: January 2021
• Est. primary completion date: January 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Women diagnosed with missed abortion during the first trimester of pregnancy

Exclusion Criteria:

• Women diagnosed with missed abortion after the first trimester of pregnancy

• Any contraindication for hysteroscopy

Related Conditions & MeSH terms

• Abortion, Missed

Intervention

Procedure:
• Fetoscopy
Fetoscopy is a procedure that enables viewing of the fetus through use of a hysteroscope

Locations

Country	Name	City	State
Israel	Hille Yaffe Medical Center	Hadera

Sponsors (1)

Lead Sponsor	Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Macroscopic anatomic malformations in missed abortions	The number and type of macroscopic anatomic malformations in missed abortions will be determined through visual observation using a fetoscope	Two years
Secondary	Minimize intrauterine adhesions through observation	To minimize intrauterine adhesions that might occur after curettage through the ability to visualize the womb and pregnancy site through a hysteroscope before the surgical procedure so that inadvertent intrauterine adhesions are minimized. After one year, if pregnancy is not achieved (due to intrauterine adhesions that cause infertility), a follow-up hysteroscopy will be performed and intrauterine adhesions can be visualized if they have occurred.	Two years
Secondary	Prevention of retained conception products	Prevention of retained conception products by hysteroscopy after curettage and visualization and observation of the contents of the womb	Two years