Sonosalpingography After Hysteroscopic Tubal Occlusion

Fallopian Tube Occlusion Clinical Trial

Official title:

Sonosalpingography in Assessment of Efficacy of Hysteroscopic Tubal Occlusion by Roller Ball Electrode

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03116867
• Other study ID #: Ainshams528
• Status: Recruiting
• Phase: N/A
• First received: April 5, 2017
• Last updated: April 12, 2017
• Start date: May 2017
• Est. completion date: April 2018

Study information

• Verified date: April 2017
• Source: Ain Shams University
• Contact: Sherif H Hussain, MD
• Phone: 0201005219239
• Email: docsherif77[@]yahoo.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Sonosalpingography is done to assess the efficacy of hysteroscopic tubal occlusion by roller ball electrode.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 56
• Est. completion date: April 2018
• Est. primary completion date: April 2018
• Gender: Female
• Age group: 20 Years to 40 Years

Eligibility

Inclusion Criteria:

• Infertile patients with hydrosalpinges requiring in vitro fertilization

• irreversible contraception

Exclusion Criteria:

• Acute pelvic inflammatory disease

Related Conditions & MeSH terms

• Fallopian Tube Occlusion

Intervention

Other:
• sonosalpingography
transvaginal ultrasound with saline infusion

Locations

Country	Name	City	State
Egypt	Ain Shams Maternity Hospital	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The presence of fluid in douglas pouch detected by transvaginal ultrasound after saline infusion through the cervix	after saline infusion is done, presence of fluid in douglas pouch means that hysteroscopic occlusion of tubes was not successful.	immediate