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NCT04396483 Clinical Trial

Dysfunctional Uterine Bleeding After Tubal Sterilization

Contraception Clinical Trial

Official title:
Dysfunctional Uterine Bleeding After Tubal Sterilization and Salpingectomy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04396483
Other study ID # DUBATS
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date March 31, 2024

Study information
Verified date November 2023
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, the investigators will compare the frequency and amount of bleeding after tubal sterilization and salpingectomy

Description:

Dysfunctional uterine bleeding is common after tubal sterilization. The investigators will compare the frequency and amount of bleeding after two techniques eithe tubal sterilization by pomeroy's method during cesarean section or complete salpingectomy

Recruitment information / eligibility
Status Recruiting
Enrollment 220
Est. completion date March 31, 2024
Est. primary completion date March 31, 2024
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - Age 20-40 - Patient completed her family - Patient on cesarean delivery Exclusion Criteria: - Tubal sterilization by other methods - Salpingectomy by laparoscopy - Patient wishing fertility

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Pomeroy's tubal sterilization
Both Fallopian tubes will be grasped by allis forceps and a kokher forceps will be applied below the allis forceps then excision of tubal part above kokher and transfixation of both ends away from each other during cesarean section
• Salpingectomy
Both fallopian tubes will be completely removed during cesarean section

Locations
Country Name City State
Egypt Adel Elgergawy Tanta Gharbia
Egypt Ayman Shehata Dawood Tanta Gharbia

Sponsors (1)
Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Frequency of Dysfunctional bleeding percentage of cases suffering of dysfunctional bleeding 1 year after cesarean section
Primary Amount of bleeding number of sanitary pads during bleeding 1 year after cesarean section
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