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Infertility clinical trials

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NCT ID: NCT01472861 Terminated - Infertility Clinical Trials

Autologous Endometrial Coculture (AECCT)

AECCT
Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of Autologous Endometrial Coculture (AECC) in young in vitro fertilization (IVF) patients with poor ovarian reserve improves pregnancy outcome.

NCT ID: NCT01443546 Terminated - Infertility Clinical Trials

Study of Dual Trigger Ovulation in Oocyte Donors

DUALTRIGGER
Start date: January 2013
Phase: Phase 4
Study type: Interventional

The project is a randomized, controlled, prospective study of oocyte donors comparing the safety and efficacy of triggering ovulation using a combination of two drugs—GnRH agonist and very low dose hCG—versus triggering ovulation with a standard hCG dose alone or a standard GnRH trigger alone.

NCT ID: NCT01419743 Terminated - Infertility Clinical Trials

Effect of Vitamin D Supplementation on In-vitro Fertilization (IVF) Outcomes

Start date: August 2011
Phase: Phase 2
Study type: Observational

Historically, vitamin D has been considered to play a role solely in bone and calcium metabolism. Numerous studies have suggested a link between vitamin D deficiency and adverse health outcomes such as malignancy, cardiovascular disease, immune functioning, and glucose metabolism. In the obstetrics literature, vitamin D deficiency has been linked to preeclampsia, gestational diabetes, and increased rate of cesarean section rate. Recent data from retrospective chart reviews have demonstrated a possible role of vitamin D in implantation and clinical pregnancy rates in patients undergoing in-vitro fertilization. Patients found to be deficient in vitamin D were found to have significantly lower clinical pregnancy rates when compared to patients who were replete in vitamin D levels. Currently, there are no prospective clinical trials investigating the effects of vitamin D supplementation on IVF outcomes such as clinical pregnancy rate and implantation rates. The investigators hypothesize that the vitamin D supplementation in patients found to be either deficient or insufficient in vitamin D will lead to improved pregnancy rates in infertility patients undergoing in-vitro fertilization.

NCT ID: NCT01332643 Terminated - Infertility Clinical Trials

Preimplantation Genetic Diagnosis (PGD) by Array Comparative Genome Hybridization (CGH) and Blastocyst Biopsy

Start date: April 2011
Phase: Phase 3
Study type: Interventional

This study evaluates the effect of single embryo transfer (SET) with and without array CGH for the evaluation of the complete chromosome complement of the blastocyst. Patients will be allocated at random into two groups. The control group will consist of patients in which one embryo will be replaced on day 5 based on morphological and developmental characteristics, and the other embryos reaching blastocyst stage will be vitrified. The test group will consist of patients undergoing embryo biopsy at the blastocyst stage (day 5 of development, embryo freezing, and analysis of the biopsied cells with a comprehensive chromosome analysis technique (array Comparative Genome hybridization or aCGH). Only a chromosomally normal blastocyst will be replaced in a thawed cycle. Inclusion and exclusion criteria are described in the study population section.

NCT ID: NCT01331395 Terminated - Clinical trials for Secondary Female Infertility

Effect of Traditional Chinese Medicine on In Vitro Fertilization (IVF) Success Rates

TCM-P002
Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the value of combining Traditional Chinese Medicine (TCM) Protocols including acupuncture with In Vitro Fertilization (IVF).

NCT ID: NCT01322971 Terminated - Infertility Clinical Trials

Efficacy Study of Preconception Treatment of an Asymptomatic Bacterial Infection in an Infertility Population

Start date: February 2011
Phase: N/A
Study type: Interventional

Bacterial vaginosis (BV) is a common vaginal infection characterized by a pathologic shift in the normal vaginal flora. BV has been associated with a number of poor reproductive outcomes, including infertility, preterm labor and premature rupture of membranes. If BV does disrupt normal embryologic development, then the treatment of BV prior to conception may improve implantation rates and other pregnancy outcomes in the infertile population. This is a prospective, randomized, double-blind, placebo-controlled trial in which infertile women undergoing intrauterine insemination or embryo transfer are screened for BV prior to treatment. Those patients who screen positive for BV will then be randomized into the treatment arm(metronidazole 500mg by mouth twice daily for 7 days) or the control arm (placebo by mouth twice daily for 7 days). The primary outcome, positive pregnancy test rate (i.e. biochemical pregnancy rate), will then be assessed. Secondary outcomes, such as clinical pregnancy rate, miscarriage rate, and live birth rate will also be examined.

NCT ID: NCT01298128 Terminated - Infertility Clinical Trials

NuvaRing vs. Oral Contraceptive Pills (OCP) for In-Vitro Fertilization (IVF) Pre-treatment

Start date: February 2006
Phase: N/A
Study type: Interventional

The newly designed contraceptive ring, Nuvaring has a lower total steroid dose, and medications are delivered locally. It has been proven to be as safe and effective as the combined OCP in ovarian suppression and preventing ovulation with fewer side effects due to minimal systemic absorption. Following a single vaginal insertion, steroid concentrations remain stable for up to 4 weeks. It is hypothesized that Nuvaring may, therefore lead to better compliance, tolerability and acceptance by patients requiring ovarian suppression prior to COH for IVF.

NCT ID: NCT01296230 Terminated - Infertility Clinical Trials

Varicocelectomy: Can Sex-hormones Predict Improvements in Semen Quality?

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the pre-operative levels of sex-hormones can be used to identify the varicocele patients who can expect improvements in their semen parameters following varicocelectomy.

NCT ID: NCT01228474 Terminated - Infertility Clinical Trials

Single Embryo Transfer vs. Double Embryo Transfer in an Oocyte Donation Programme

Start date: October 2010
Phase: N/A
Study type: Interventional

Experimental study to assess the efficacy of single embryo transfer (SET) with respect to double embryo transfer (DET) in an oocyte donation programme, 160 recipients will be randomized in two groups

NCT ID: NCT01208740 Terminated - Infertility Clinical Trials

Metformin in Patients With PCOS and Predictors of Poor Ovarian Response Ongoing In-vitro Fertilization

Start date: January 2009
Phase: Phase 4
Study type: Interventional

Metformin should be administered with caution and could be potentially dangerous in infertile patients with PCOS who show a poor ovarian response and are undergoing gonadotropin-based ovarian stimulation. However, data that address this point are totally lacking. On the basis of these considerations, the aim of the current clinical trial was to test the hypothesis that metformin reduces the ovarian response in infertile patients with PCOS who have a potentially poor ovarian response and who undergo gonadotropin stimulation for IVF cycles.