Sonosalpingography After Hysteroscopic Tubal Occlusion
Sonosalpingography in Assessment of Efficacy of Hysteroscopic Tubal Occlusion by Roller Ball Electrode
1 other identifier
observational
56
1 country
1
Brief Summary
Sonosalpingography is done to assess the efficacy of hysteroscopic tubal occlusion by roller ball electrode.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2017
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 5, 2017
CompletedFirst Posted
Study publicly available on registry
April 17, 2017
CompletedStudy Start
First participant enrolled
May 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2018
CompletedApril 17, 2017
April 1, 2017
11 months
April 5, 2017
April 12, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
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
Study Arms (1)
patients receiving hysteroscopic tubal occlusion
This group will have sonosalpingography done for them one month after the tubal occlusion.
Interventions
transvaginal ultrasound with saline infusion
Eligibility Criteria
patients requiring tubal occlusion
You may qualify if:
- Infertile patients with hydrosalpinges requiring in vitro fertilization
- irreversible contraception
You may not qualify if:
- Acute pelvic inflammatory disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ain Shams Maternity Hospital
Cairo, Egypt
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
April 5, 2017
First Posted
April 17, 2017
Study Start
May 1, 2017
Primary Completion
April 1, 2018
Study Completion
April 1, 2018
Last Updated
April 17, 2017
Record last verified: 2017-04
Data Sharing
- IPD Sharing
- Will not share