Pregnancy Rate After Unilateral Tubal Disconnection

NCT ID: NCT04389203

Last Updated: 2023-11-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

110 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-01

Study Completion Date

2024-06-30

Brief Summary

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Unilateral disconnection of one tube that had hydrosalpinx

Detailed Description

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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

Conditions

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Pregnancy Rate

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Unilateral tubal disconnection and spontaneous pregnancy
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Study group

Unilateral tubal disconnection and waiting for pregnancy for 2 years after laparoscopy

Group Type EXPERIMENTAL

Unilateral tubal disconnection + Spontaneous follow up for pregnancy

Intervention Type PROCEDURE

Unilateral tubal disconnection + Spontaneous follow up for pregnancy

Control group

Unilateral tubal disconnection and ICSI

Group Type EXPERIMENTAL

Unilateral tubal disconnection + ICSI

Intervention Type PROCEDURE

Unilateral tubal disconnection + ICSI

Interventions

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Unilateral tubal disconnection + Spontaneous follow up for pregnancy

Unilateral tubal disconnection + Spontaneous follow up for pregnancy

Intervention Type PROCEDURE

Unilateral tubal disconnection + ICSI

Unilateral tubal disconnection + ICSI

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* infertile women either primary or secondary Hydrosalpinx

Exclusion Criteria

* other factors of infertility
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Tanta University

OTHER

Sponsor Role lead

Responsible Party

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Ayman S Dawood, MD

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Adel Elgergawy

Tanta, Gharbia Governorate, Egypt

Site Status RECRUITING

Countries

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Egypt

Facility Contacts

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Adel Elgergawy, MD

Role: primary

+201002057250

Other Identifiers

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PRAUTD

Identifier Type: -

Identifier Source: org_study_id