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Female Infertility clinical trials

View clinical trials related to Female Infertility.

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NCT ID: NCT03057574 Recruiting - Female Infertility Clinical Trials

Gonapure® in Multifollicular Stimulation in Egyptian Women Undergoing IVF/ICSI

GIVF
Start date: February 9, 2017
Phase: Phase 4
Study type: Interventional

This study aims to record Efficacy, Safety and tolerability of Gonapure® prescribed for female subjects with infertility Undergoing IVF/ICSI

NCT ID: NCT03045315 Recruiting - Female Infertility Clinical Trials

LXR and Oocyte Meiosis Resumption

Start date: January 2015
Phase: N/A
Study type: Interventional

Previous studies in animal model showed clearly that lipid homeostasis influence oocyte meiosis resumption. However Liver X Receptors pathway has never been investigated in human ovocyte

NCT ID: NCT02918812 Recruiting - Clinical trials for Female Infertility of Tubal Origin

Intracervical Lidocaine Versus Intramuscular Diclofenac for Pain Relief in HSG in a Tertiary Hospital in Kano

Start date: September 2016
Phase: Phase 4
Study type: Interventional

This study compares the effect of intracervical block with 1% lidocaine and intramuscular diclofenac 75mg in decreasing pain perception during hysterosalpingography. Half of participants will receive intracervical block with 1% lidocaine, while the other half will receive intramuscular diclofenac 75mg.

NCT ID: NCT02802397 Completed - Female Infertility Clinical Trials

AROPE : Early Ovarian Reserve Decreased : Impact of Exposure to Persistent Endocrine Disruptors and Organic Solvents

AROPE
Start date: December 6, 2016
Phase: N/A
Study type: Interventional

Early ovarian reserve decreased is one of the main causes of infertility for women after 35 years. The relationship between this decreased and exposure to chemicals, including persistent endocrine disruptors or organic solvents, has been little studied. However, several in vivo or in vitro experimental studies suggested that these chemicals may impaired ovarian function. The main objective is to study the relationship between early ovarian reserve decreased and exposure to persistent organic pollutants. The secondary objectives are to study the relationship between early ovarian reserve decreased and exposure to organic solvents and heavy metals. Multicenter case-control study. This project will permit to increase the knowledge concerning the etiology of early decreased ovarian reserve. Considering that exposure of interest are frequent, the results may be important in a public health perspective. If associations are observed in this study, the results may encouraged prevention strategy.

NCT ID: NCT02775877 Recruiting - Clinical trials for Female Infertility Due to Nonimplantation of Ovum

Letrozole and Sequential Clomiphene to Improve the Outcome of Embryo Transfer

Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to study the effects of letrozole and sequential clomiphene in ovulation and pregnancy in PCOS patients.

NCT ID: NCT02741102 Not yet recruiting - Female Infertility Clinical Trials

Uterine Transplant in Absolute Uterine Infertility (AUIF)

Start date: June 2016
Phase: N/A
Study type: Interventional

This study will examine the feasibility of initiating a uterine transplant program for Absolute Uterine Factor Infertility (AUFI) at Brigham and Women's Hospital. The investigators plan to screen 30 patients with a goal of enrolling 10 patients. (5 donors and 5 recipients) After careful screening, appropriate candidates will undergo IVF, Uterine Transplantation, Embryo Transfer, Pregnancy and Delivery. Once the uterus is explanted, five years of follow-up is planned.

NCT ID: NCT02727400 Completed - Clinical trials for Female Infertility Due to Advanced Maternal Age

Mitochondrial Energy Production in ART (Assisted Reproductive Technology )

Mitenergy
Start date: April 1, 2017
Phase:
Study type: Observational

Oocyte maturation requires a lot of energy, which is provided by the mitochondria via the synthesis of ATP. The majority of patients with advanced maternal age (AMA) have poor egg quality. One of the reasons depends on oxidative phosphorylation of Pyruvate to undergo maturation; on the contrary, the cells of the cumulus (CC) show great activity glycolytic so that these cells are able to provide ATP(adenosine triphosphate and energy substrates to the oocyte. The goal of this work is to analyze the mitochondrial function and energy production in oocyte donors compared with a group of women of advanced maternal age subject to a same ovarian stimulation Protocol

NCT ID: NCT02696330 Recruiting - Clinical trials for Female , Infertility

Comparison Between Effect of Enoxaparin and Clopidogrel on Improving Pregnancy Rate in ICSI

Start date: September 2015
Phase: Phase 4
Study type: Interventional

Comparison between effect of enoxaparin and clopidogrel on improving pregnancy rate in ICSI

NCT ID: NCT02640261 Recruiting - Female Infertility Clinical Trials

Observational Prospective Study of the Success of Single Embryo Transfer Implantation Related to Level of Follicular Fluid Cytokines Expression in Low Responders Infertile Patients Treated With r-hLH add-on Therapy in a Second Controlled Ovarian Stimulation Cycle.

Start date: January 2016
Phase: N/A
Study type: Observational

The objective of our observational prospective study will be to compare, for women treated for infertility and included in a ICSI program, the implantation rate and delivery rate obtained after the transfer of a single blastocyst , chosen in a group of patients on the basis of the embryo morphology and in the other group on the basis of both embryo morphology and follicular fluid cytokines content. 100 IVF infertile patients , aged 32-39 years, with normal ovarian reserve, previously stimulated for their first cycle with standard short protocol (GnRH-Ant) and r-FSH alone, who have had a low ovarian response, Fort < 50% ( FORT Criteria, 2012; FORT= PFCX100/AFC), will be treated for the second cycle with standard short protocol (GnRH-Ant) and r-FSH plus r-LH , according to the standard established by our clinical practice. Patients will be part of one of the following groups: Group 1: single embryo transfer on day 5, according to standard embryo morphological criteria Group 2: single embryo transfer on day 5, chosen on the basis of both embryo morphological criteria and levels of cytokines measured in the individual FF.

NCT ID: NCT02544776 Completed - Clinical trials for Female Infertility Associated With Anovulation

Amlodipine on Blood Flow of Preovulatory Follicle in Polycystic Ovarian Patients

Start date: January 2015
Phase: N/A
Study type: Interventional

On the basis of the current study, amlodipine seems to be a promising drug on improving uterine, ovarian blood flow, size of pre-ovulatory follicle, midluteal progesterone level and pregnancy outcome in patients with pco.