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NCT04389203 Clinical Trial

Pregnancy Rate After Unilateral Tubal Disconnection

Pregnancy Rate Clinical Trial

Official title:
Pregnancy Rate After Laparoscopic Unilateral Tubal Disconnection

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04389203
Other study ID # PRAUTD
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date June 30, 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

Unilateral disconnection of one tube that had hydrosalpinx

Description:

In cases suffering from infertility and all other factors were normal except hysterosalpingogram that showed hydrosalpinx. We either did intracytoplasmic sperm injection (ICSI) in one group and spontaneous follow up for 2 years after laparoscopy Pregnancy rate in both groups was assessed

Recruitment information / eligibility
Status Recruiting
Enrollment 110
Est. completion date June 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - infertile women either primary or secondary Hydrosalpinx Exclusion Criteria: - other factors of infertility

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Unilateral tubal disconnection + Spontaneous follow up for pregnancy
Unilateral tubal disconnection + Spontaneous follow up for pregnancy
• Unilateral tubal disconnection + ICSI
Unilateral tubal disconnection + ICSI

Locations
Country Name City State
Egypt Adel Elgergawy 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 Pregnancy rate Number of pregnant women after procedure 2 years
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