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Infertility clinical trials

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NCT ID: NCT02806934 Completed - Infertility Clinical Trials

TNF Polymorphism and Implantation Rate

Start date: June 2009
Phase: N/A
Study type: Observational

Do TNF-308 and -238 polymorphisms impact the embryo implantation rate after in vitro fertilization (IVF) in women without female infertility factor ?

NCT ID: NCT02802865 Completed - Infertility Clinical Trials

Combined Letrozole and Clomid in Women With Infertility and PCOS

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

This study evaluates the addition of clomid to letrozole for the treatment of infertility in women with polycystic ovary syndrome. Half of the participants will receive letrozole and clomid in combination, while the other half will receive letrozole alone.

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: NCT02798146 Completed - Infertility Clinical Trials

Early Luteal Progesterone Profile After hCG Triggering

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

This pilot-study will help characterize the serum progesterone profiles in IVF patients and correlate progesterone levels to ovarian follicles obtained after stimulation with exogenous gonadotropins.

NCT ID: NCT02796105 Completed - Infertility Clinical Trials

Progevera 10 mg® Versus Orgalutran® in Ovarian Stimulation Cycles of Oocyte Donors

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

Evaluation of efficacy and safety of medroxiprogesterone acetate (Progevera 10 mg®) versus GnRh antagonist (Orgalutran®) in ovarian stimulation cycles of oocyte donors

NCT ID: NCT02793752 Completed - Infertility Clinical Trials

Mitochondrial Activity of Cumulus Cells From the Cumulus-oocyte Complex and Oocyte Competence

Start date: March 2016
Phase:
Study type: Observational

The need for non-invasive biomarkers of oocyte competency has become urgent as women increasingly delay attempts at childbearing. The aging process is complex and includes impaired mitochondrial dysfunction, oxidative stress, diminished metabolic activity, and activity of several cell-signaling systems. Cumulus cells form an intimate association with the oocyte in the follicle, and they can have a significant impact on oocyte meiotic and developmental competence. In the IVF lab, the clump of cumulus cells is typically cut away from the oocyte immediately after an oocyte retrieval procedure, and then the cumulus cells are discarded. Measuring the mitochondrial respiratory activity of cumulus cells may serve as a non-invasive biomarker for oocyte competency and a predictor of reproductive success in IVF patients in the future.

NCT ID: NCT02792569 Completed - Infertility Clinical Trials

Follicle Activation by Inhibition of the Hippo Pathway

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

The aim of this project is to activate recruitment and growth of resting primordial follicles in the ovaries of women with diminished ovarian reserve, in attempt to increase the chance to become pregnant, either naturally or after assisted reproduction.

NCT ID: NCT02788617 Completed - Infertility Clinical Trials

Evaluation of the Efficacy of Diafert in Predicting Embryos' Potential to Develop to the Blastocyst Stage

Start date: June 24, 2016
Phase: N/A
Study type: Observational

This prospective study will evaluate the efficacy of Diafert as an adjunct to morphological assessment in predicting embryos' potential to develop to the blastocyst stage on Day 5.

NCT ID: NCT02787811 Completed - Clinical trials for Assisted Reproductive Techniques

Predictors of Success of IUI in Unexplained Infertility

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

Superovulation will be conducted with 100 mg of oral clomiphene citrate (Clomifene; Young Poong Pharmaceutical, Incheon, Korea) for 5 days starting on day 3 of the menstrual cycle, followed by daily injection of 150 IU of human menopausal gonadotropin (hMG;Menogon; FerringPharamceutical Co, Germany). When more than 2 dominant follicles reached a diameter of 17 mm or the urinary specimen showed positive results for luteinizing hormone (LH) surge, 5000 IU of hCG (Pregnyl; Organon, Oss, the Netherlands) was injected intramuscularly.

NCT ID: NCT02766725 Completed - Infertility Clinical Trials

Thermosensitive Gels for the Vaginal Delivery of Sildenafil Citrate

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Start date: January 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study was to develop and characterize in situ thermosensitive gels for the vaginal administration of sildenafil as a potential treatment of the endometrial thinning that occurs as a result of the use of clomiphene citrate in induction of ovulation in women with World Health Organization type II EU gonadotrophic anovulation.