Comparing two methods of tubal sterilization during Caesarean section
Pelvic Congestion Syndrome Following Salpingectomy Compared to Tubal Ligation at Time of Caesarean Section
This study is testing whether a new surgery for permanent birth control during C-section can help women feel better and have fewer symptoms related to pelvic congestion syndrome compared to a standard method.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Ages | 30 Years and up |
| Sex | Female |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo, Abaseya) |
| Trial ID | NCT06509425 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effects of bilateral salpingectomy versus bilateral tubal ligation performed during Caesarean delivery on women seeking permanent contraception. Participants will be randomly assigned to one of the two surgical methods, with careful monitoring and follow-up assessments to evaluate outcomes related to pelvic congestion syndrome. The study aims to determine which method may offer better relief from symptoms associated with pelvic congestion syndrome, a condition that can significantly impact quality of life. The research will involve informed consent and thorough pre-operative screening to ensure participant eligibility.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 30 years or older who are undergoing a Caesarean section and requesting tubal sterilization.
Not a fit: Patients with a history of tubal surgery, oophorectomy, congenital anomalies, or those already diagnosed with pelvic congestion may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into the most effective surgical method for reducing pelvic congestion symptoms in women undergoing tubal sterilization.
How similar studies have performed: While the approach of comparing these two surgical methods is not widely tested, existing literature suggests that salpingectomy may have additional benefits over tubal ligation, particularly in relation to ovarian cancer prevention.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Females undergoing caesarean section and requesting tubal sterilization as a permanent method of contraception. * 30 years or older Exclusion Criteria: * Previous history of tubal surgery (changes in blood flow) * Previous history of oophorectomy (changes in blood flow) * Congenital anomalies or malformations in fallopian tubes or ovaries. (affection of normal anatomy of pelvic blood vessels) * Women diagnosed with pelvic congestion. (Known cause for pelvic congestion other than tubal sterilization) * High likelihood of lost to follow up. * Inability to provide good data.
Where this trial is running
Cairo, Abaseya
- Ain Shams Maternity Hospitals — Cairo, Abaseya, Egypt (Recruiting)
Study contacts
- Study coordinator: Mayar Z Kamal
- Email: mayarziad2@gmail.com
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.