The value of ultrasound guidance during IUD insertion in women with RVF uterus: A randomized controlled trial.

Objective: The study objective is to evaluate the benefits of using ultrasound guidance during insertion of Intrauterine device IUD in women with retroverted flexed RVF uteri.

Study Design: A randomized controlled trial conducted on 400 women with RVF uteri eligible for IUD insertion. They were randomly divided into 2 groups.

Diagnostic accuracy of posterior cervical angle and cervical length in the prediction of successful induction of labor.

Objective: To determine the accuracy of the posterior cervical angle (PCA) compared with the cervical length and the Bishop score in predicting the outcome of induction of labor (IOL).

Methods: The present prospective observational study included IOL candidates who had their PCA and cervical length assessed by transvaginal ultrasonography and the Bishop score at the Obstetrics and Gynecology Department, Kasr El-Aini Hospital, Cairo University, Cairo, Egypt, between April 1 and July 31, 2017. The accuracy of these tests in predicting successful IOL (defined as vaginal delivery) was compared.

Effect of laser-assisted zona thinning, during assisted reproduction, on pregnancy outcome in women with endometriosis: randomized controlled trial.

Objective: To compare the ICSI-ET outcomes in patients with endometriosis with or without laser-assisted zona pellucida thinning.

Design: Randomized controlled trial.

Setting: The study was conducted in the Obstetrics & Gynecology Department, Cairo University hospital, and two private IVF centers in Cairo & Beni-Suif from July 2015 to January 2017 upon infertile and known endometriosis patients who planned to do ICSI-ET.

Cervical Priming by Vaginal or Oral Misoprostol Before Operative Hysteroscopy: A Double-Blind, Randomized Controlled Trial.

Study Objective: To evaluate whether misoprostol oral is as effective as vaginal tablets for cervical ripening.

Design: Randomized controlled trial involving a parallel, double-blinded study (Canadian Task Force Classification IB).

Setting: Department of Obstetrics and Gynecology, Cairo University Hospital, between January 2014 and January 2016.

Antagonist protocol versus clomiphene in unexplained infertility: A randomized controlled study.

Objective: The primary purpose of this randomized controlled trial study was to compare clinical pregnancy rates and ovulation parameters in female patients of unexplained infertility undergoing intrauterine insemination (IUI) using an antagonist protocol versus a conventional clomiphene citrate protocol.

Materials And Methods: This was a multicenter parallel randomized controlled, open-label trial. A central randomization center used computer generated tables to allocate treatments.

Delayed Start Versus Conventional GnRH Antagonist Protocol in Poor Responders Pretreated With Estradiol in Luteal Phase: A Randomized Controlled Trial.

Objective: To compare the new delayed start protocol against the conventional gonadotropin (Gn)-releasing hormone antagonist protocol in poor responders (PORs).

Study Design: A total of 160 women with poor response to previous in vitro fertilization (IVF) cycle were randomized either to start Gn then Cetrotide 0.25 subcutaneously (sc) added when leading follicle (DF) reach >12 mm or Cetrotide 0.