Completed

ETEffect of Ultrasound Guided Embryo Transfer on Pregnancy Rates

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

GnRh, HMG, HCG, Progesterone

+ GnRh, HMG, HCG, Progesterone

Drug
Who is being recruted

Urogenital Diseases

+ Genital Diseases

+ Infertility

From 20 to 39 Years
+9 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-Controlled
Interventional
Study Start: September 2009
See protocol details

Summary

Principal SponsorAin Shams Maternity Hospital
Last updated: March 26, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2009

Actual date on which the first participant was enrolled.

A total of 90 patients undergoing treatment with ICSI were divided into 2 groups: group 1 (45 patients), had ultrasound guided embryo transfer and group 2 (45 patients), underwent embryo transfer using the clinical touch technique

Principal SponsorAin Shams Maternity Hospital
Last updated: March 26, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

90 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 20 to 39 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesGenital DiseasesInfertility

Criteria

4 inclusion criteria required to participate
Age (20-39)

Male factor infertility

Ovarian factor infertility

Unexplained infertility

5 exclusion criteria prevent from participating
Difficult embryo transfer

Endometriosis

FSH > 16 iu/l on cycle day 3

Less than 2 embryos grade A

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
GnRh, HMG, HCG, Progesterone 45 patients had ultrasound guided embryo transfer during ICSI

Group II

Placebo
GnRh, HMG, HCG, Progesterone 45 patients had embryo transfer using clinical touch technique during ICSI

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

IVF Unit, Ain Shams Maternity Hospital, Ain Shams University

Cairo, EgyptOpen IVF Unit, Ain Shams Maternity Hospital, Ain Shams University in Google Maps
CompletedOne Study Center