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Infertility, Male clinical trials

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NCT ID: NCT02932865 Completed - Infertility, Male Clinical Trials

Modern Analyses of the Semen in Evaluating Male Fertility and Treatment Options of Male Infertility

SemiFluid
Start date: November 2016
Phase:
Study type: Observational

Men are recruited to collect seminal plasma samples and serum samples from men with azoospermia, men receiving medical treatment of infertility and men attending semen analysis. MicroRNA (miRNA) and PiWi-interacting RNA (piRNA) are analyzed for all of the groups to find potential differences. Steroid hormones are analyzed by liquid chromatography-tandem mass spectrometry.

NCT ID: NCT02931721 Completed - Male Infertility Clinical Trials

Treatment of Severe Male Infertility - Predictive Factors (Imaging)

TESE-MRI
Start date: November 1, 2016
Phase:
Study type: Observational

Testes of men with non-obstructive azoospermia (NOA) are imaged using MRI to find potential differences depending on the outcome, ie. sperm recovery in consequent microdissection testicular sperm extraction (MD-TESE).

NCT ID: NCT02889341 Completed - Male Infertility Clinical Trials

Valuation of Variable Dose of Docosahexanoic Acid for the Improvement of the Parameters of Male Fertility

DHA
Start date: October 22, 2013
Phase: N/A
Study type: Interventional

Sperm parameters will be examined before DHA (DHA=Docosahexanoic Acid) consumption, after one months and after 2 months taken Docosahexanoic Acid or placebo.

NCT ID: NCT02814695 Completed - Infertility, Male Clinical Trials

Yeast Cells as Antioxidant-Producing Probiotics

Probiotics
Start date: August 15, 2020
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the efficacy of Baker's yeast extractions , probiotic antioxidant, in scavenging the oxidative stress status mediated damage on sperm motility,progressive motility and vitality as well as comparing this potency to that of Vitamin E in infertile men.

NCT ID: NCT02756923 Completed - Male Infertility Clinical Trials

Regulation of Stem Spermatogonia in the Mature Testis

Start date: April 2012
Phase:
Study type: Observational

Investigative trial to evaluate the role of a glial cell lined derived neurotrophic factor (GDNF) in regulation of spermatogonial renewal and testicular function. Goal of the trial is to provide greater information on the mechanisms that effect stem spermatogonial maintenance renewal and proliferation in its relation to male infertility.

NCT ID: NCT02475395 Completed - Sub-Fertility, Male Clinical Trials

Study of the Consumer Use of a New Home Test to Measure Sperm Concentration

Start date: September 2, 2015
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate the agreement in measurement of sperm concentration in human semen between lay users with TRAK and a recognized reference method. The study will also include the measurement of matched samples by TRAK when tested by healthcare professionals trained in use of the TRAK device.

NCT ID: NCT02421887 Completed - Male Infertility Clinical Trials

Males, Antioxidants, and Infertility Trial

MOXI
Start date: December 2015
Phase: Phase 2
Study type: Interventional

The objective of the Males, Antioxidants, and Infertility (MOXI) Trial is to examine whether treatment of infertile males with an antioxidant formulation improves male fertility. The central hypothesis is that treatment of infertile males with antioxidants will improve sperm structure and function, resulting in higher fertilization rates and improved embryo development, leading to higher pregnancy and live birth rates. Findings from this research will be significant in that they will likely lead to an effective, non-hormonal treatment modality for male infertility. An effective treatment for men would also reduce the treatment burden on the female partner, lower costs, and provide effective alternatives to couples with religious or ethical contraindications to ART (Assisted Reproductive Technology). If antioxidants do not improve pregnancy rates, but do improve sperm motility and DNA integrity, they could allow for couples with male factor infertility to use less intensive therapies such as intrauterine insemination. Male fertility specialists currently prescribe antioxidants based on the limited data supporting their use. A negative finding, lack of any benefit, would also alter current treatment of infertile males.

NCT ID: NCT02349945 Completed - Male Infertility Clinical Trials

FSH Receptor Polymorphism p.N680S and Efficacy of FSH Therapy

Start date: January 2011
Phase: Phase 2/Phase 3
Study type: Interventional

CONDITION: Idiopathic male infertility In men with idiopathic infertility, the sperm DNA fragmentation index (DFI) within 12 weeks of FSH therapy and 12 weeks follow-up improves depending on the FSHR genotype as assessed by the non-synonymous SNP rs6166 (wild type or p.N680S). This is a phase II b, multicenter, prospective, open label, one arm, clinical trial stratified according to the patient's genotype. INTERVENTION: FSH therapy (150 I.U. sc every other day for 12 weeks) in infertile men who are homozygous for the wild-type FSHR or the p.N680S allele of the FSHR. Duration of intervention per patient: 12 weeks Primary efficacy endpoint: Sperm DFI. Number of patients with an improvement in DFI > 60% Key secondary endpoint(s): pregnancy, semen parameters, serum levels of inhibin B and AMH.

NCT ID: NCT02310087 Completed - Infertility, Male Clinical Trials

Oral Astaxanthin and Semen Quality, Fertilization and Embryo Development in Assisted Reproduction Techniques Procedures

Astax-ART
Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether administration of dietary supplement of astaxanthin with vitamin E improves the quality of sperm, fertilization and embryo development in Assisted Reproduction Techniques (ART) procedures.

NCT ID: NCT02272439 Completed - Male Infertility Clinical Trials

Endocrine Disrupting Chemicals: Potential Effects on Male and Female Reproductive Health in Saskatchewan

Start date: March 2012
Phase: N/A
Study type: Observational [Patient Registry]

The overall objective of this study is to determine whether serum BPA and/or phthalate concentrations differ in fertile versus infertile men and women in Saskatchewan. The investigators will test the following hypothesis: 1. Serum BPA and/or phthalate concentrations will be greater in women with unexplained infertility or PCOS compared to a control group 2. Serum BPA and/or phthalate concentrations will be greater in men with male factor infertility compared to a control group