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Infertility clinical trials

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NCT ID: NCT02458963 Withdrawn - Infertility Clinical Trials

IVF Versus Gonadotropin Therapy in Women With CC Resistant PCOS

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

The purpose of this study is to compare the efficacy of in vitro fertilization (IVF) versus gonadotropin therapy in infertile women having clomiphene citrate (CC) resistant polycystic ovarian syndrome (PCOS).

NCT ID: NCT02456792 Withdrawn - Infertility Clinical Trials

IVF Versus LOD in Women With CC Resistant PCOS

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

The purpose of this study is to compare the efficacy of in vitro fertilization (IVF) versus laparoscopic ovarian drilling (LOD) in infertile women having clomiphene citrate (CC) resistant polycystic ovarian syndrome (PCOS).

NCT ID: NCT02377479 Withdrawn - Infertility Clinical Trials

Endocrinology Profile in Patients Undergoing Clomiphene, Letrozole, and Combination Clomiphene and Letrozole Cycles

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

The goal of the study is to measure serial hormonal levels in patients undergoing clomiphene, letrozole, and a combination clomiphene and letrozole cycle. This information may help us to optimize less expensive medications for ovulation induction, reduce the number of treatment cycles to achieve a successful pregnancy, and use a medication regimen that may result in fewer multiple gestation pregnancies.

NCT ID: NCT02341339 Withdrawn - Infertility Clinical Trials

Utility of Fallopian Tube Cocultures in Assisted Reproductive Technology

Start date: n/a
Phase: N/A
Study type: Interventional

Prospective Feasibility Study: Fallopian tube cells will be obtained from patients undergoing laparoscopic surgery during their surgical evaluation of infertility. Of note, these patients are already scheduled to undergo surgery as part of their standard of care.

NCT ID: NCT02328742 Withdrawn - Infertility Clinical Trials

Development of a Bioabsorbable Medical Device for the Prevention of Postoperative Intra-uterine Adhesions.

PréSynUT-1
Start date: November 2015
Phase: N/A
Study type: Observational

The main objective of this study is to describe the level of expression of the biological factors involved in the formation of adhesions (Transforming growth factor beta, Activin A, inhibin) at the time of a first diagnostic hysteroscopy among women with synechia, another intracavitary disease or no intracavitary disease.

NCT ID: NCT02209168 Withdrawn - Clinical trials for Vitamin D Deficiency

Differences in Ovarian Reserve Markers and Vitamin D Between Infertile Indian, Arabian and Caucasian Population

Start date: November 2015
Phase:
Study type: Observational

The aim of this study is to confirm the difference in ovarian reserve markers and serum vitamine D levels between infertile indian, arabian and caucasian population.

NCT ID: NCT02160704 Withdrawn - Infertility Clinical Trials

Androxal in Male Infertility

Start date: September 22, 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This is an exploratory, single center, randomized, parallel, double-blind placebo- and active-controlled trial in adult males ages 18 to 35 years of age who have male infertility of unknown cause. Approximately 50 men will be randomly assigned to one of two treatment groups according to a 1:1 ratio. About half of the men will receive 25mg Androxal and half of the men will receive a placebo (non-active pill) for 16 weeks. This study will last approximately 4 months and involve up to 7 visits. The purpose of this study is to determine the effect the Androxal on sperm production.

NCT ID: NCT02051075 Withdrawn - Infertility Clinical Trials

Fertilizations With Immotile Sperm: Pentoxyphylline Activation Alone, or With Chemical Oocyte Activation

PXN
Start date: March 2014
Phase: Phase 4
Study type: Interventional

Immotile sperm is a rather frequent problem encountered in IVF patients. Treatment is usually based on inducing motility with pentoxyphylline (PXN) followed by ICSI. However, fertilization rate with this method is still lower compared with ICSI using motile sperm. One of the reasons for that is the immotile sperm inability to activate the oocyte Our research hypothesis is that better fertilization rate can be accomplished in these cases by combining PXN sperm activation with Ca ionophore oocyte activation.

NCT ID: NCT02028897 Withdrawn - Infertility Clinical Trials

Comparison of Alternative Embryo Culture Systems

Start date: n/a
Phase: N/A
Study type: Interventional

This study will compare two alternative embryo culture systems. Embryos from each patient will be randomly assigned to one of two systems. One group will be cultured conventionally in oil-covered droplets in dishes. The other group will be assigned to an enclosed system.

NCT ID: NCT01971060 Withdrawn - Infertility Clinical Trials

a Study to Evaluate Adhesion Risk in Fertility Patients' Status Post Laparoscopic Myomectomy.

VLocmyo
Start date: August 2013
Phase: N/A
Study type: Interventional

Premenopausal Women ages 18-42 will undergo a laparoscopic myomectomy. Prior to the myomectomy, adhesions will be assessed using a modified AFS scoring technique. All investigators will provide usual and customary care to research subjects during the first look laparoscopy. This includes the use of all standard practice anti-adhesive agents and heparinized irrigation fluids.V-Loc 180 suture will be utilized in all patients. All patients will then be evaluated by means of a second look laparoscopy (SLL) 6-12 weeks after the initial surgery and reevaluated via modified American Fertility Society scoring techniques. An independent reviewer will also score adhesions utilize a video recording made from the second look laparoscopic surgery. Patients will be contacted both 1 and 4 weeks post -op and assessed for complications. It is the expectation that patients will show no greater post-operative adhesion formation and a <1% complication rate. Time and ease of suturing will also be evaluated. It is expected that the V-Loc suturing technique will show significantly reduced suturing time, be easier to use, and will be associated with minimal adhesions.