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Infertility clinical trials

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NCT ID: NCT03678571 Completed - Infertility Clinical Trials

Oocyte Vitrification Aided With Latrunculin A

Start date: September 25, 2018
Phase: N/A
Study type: Interventional

Using cytoskeleton Stabilizer the Latrunculin A would improve the outcome of oocyte vitrification

NCT ID: NCT03678558 Completed - Infertility Clinical Trials

Oocyte Vitrification Aided With Cytochalasin B

Start date: September 25, 2018
Phase: N/A
Study type: Interventional

Using the cytoskeleton Stabilizer the Cytochalasin B would improve the outcome of oocyte vitrification.

NCT ID: NCT03677492 Completed - Infertility Clinical Trials

Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin D ( ICSI-CD)

Start date: September 25, 2018
Phase: N/A
Study type: Interventional

Vienna Consensus has identified 10% damage rate after ICSI as a competency value. Despite the highest quality embryologists doing ICSI, degeneration sometimes occurs due to oocyte factors such as the fragile membrane, etc. Cytochalasin D serves to facilitate spindle or pronuclear transfer procedures helping to reduce the damage rate with no harm reported. Using Cytochalasin D during ICSI could serve to rescue some oocytes from the degeneration allowing for more chances of viable zygotes.

NCT ID: NCT03677336 Completed - Infertility Clinical Trials

Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Luteal Phase Support (LPS) in IVF/ICSI

Start date: May 1, 2019
Phase: Phase 4
Study type: Interventional

Female inability to conceive a child. The purpose of this prospective randomized, double-blinded, double dummy, two-arm cross-over study is to investigate the difference on histological, transcriptional and immunological level in endometrium between 3x10mg Dydrogesterone oral tablets and 3x200 mg Micronized progesterone intravaginal capsules for the luteal support in egg cell donors. Beside that, the pharmacokinetics, the impact on the peripheral immunology (by blood sampling) and the microbiota (by genital swabs) will be investigated.

NCT ID: NCT03677063 Completed - Peritoneal Dialysis Clinical Trials

Usefulness of Sterile Adhesive Dressing at the Exit-site of Peritoneal Dialysis Catheter

PANCADIPE
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Infection of peritoneal dialysis fluid is a major complication in patients treated with peritoneal dialysis (PD). The aim of catheter emergence care is to reduce bacterial contamination of the peritoneum. The recommendations of the International Society of Peritoneal Dialysis do not provide information on the frequency of care delivery or the usefulness of a sterile adhesive dressing. Thus each treatment center applies a protocol of its own. Dressing is common practice although its safety and interest are not demonstrated. The usefulness of dressing is still to be demonstrated. On the other hand, the efficacy of the application in prevention of a cream of mupirocin at emergence on the reduction of the risk of infection with staphylococcus aureus (SA), the most frequent germ found in peritonitis, has been demonstrated. A Spanish study showed that during a peritoneal infection at SA the site most frequently colonized by a similar strain of SA was the emergence of the catheter. It can be considered that an infection of the dialysis liquid in PD is not only related to the quality of emergency care but also to manipulations during exchanges. Given the number of patients involved in PD in France, it is difficult to obtain sufficient power to formally demonstrate the non-inferiority of the absence of dressing. Therefore, the investigators propose a descriptive, exploratory study of events that may occur in PD when a dressing is not applied. This is a step prior to performing a multicenter randomized comparative study that will aim to show the non-inferiority of the absence of dressing compared to the application of a dressing on the incidence of fluid infection. peritoneal dialysis.

NCT ID: NCT03677011 Completed - Male Infertility Clinical Trials

Andrositol® TEST as Diagnostic Assay to Predict the Fertilization Potential in IVF

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

Andrositol® test allows to obtain additional information besides the WHO parameters and to evaluate the semen energetic status. The diagnosis is performed by analyzing the semen at two different time points: before the treatment and 30' after the addiction of myo-inositol directly to the semen. The purpose of this study is to evaluate if the responsiveness to the Andrositol® test of a sperm sample can be predictive of its fertilization rate in an ICSI (Intracytoplasmic Sperm Injection) cycle (primary outcome). Secondary outcomes as embryo development, embryo euploidy status and embryo implantation rate will be evaluated.

NCT ID: NCT03669276 Completed - Infertility Clinical Trials

Effect of Gonadotropin Types and Indications on Homologous Intrauterine Insemination Success

GONADOTROP
Start date: August 1, 2014
Phase:
Study type: Observational

In this study the investigators took the opportunity of having a large sample of IUI cycles in a single centre to try to analyse the effect of stimulation protocols and of the infertility origin on the results, taking in account the main confounding variables (female age, IUI attempt rank, and sperm quality) on the clinical outcome. All couples had undergone a standard infertility evaluation, which included medical history, physical examination, and assessment of tubal patency by either hysterosalpingography or laparoscopy and hormonal analysis on cycle day 3. A transvaginal ultrasound scan was performed on the second day of the cycle. On the same day, ovarian stimulation was carried out with recombinant FSH (follitropinrFSH; Gonal-F, MerckSerono, France, orfollitropin;Puregon, MSD, France), urinary FSH (urofollitropin, Fostimon, France), orhMG (menotropin, Menopur, France) atastarting dose of 75 IU/day from the second day of the cycle. The main clinical outcome measures were clinical pregnancy and live-birth rates per cycle. Clinical pregnancy was defined as the evidence of pregnancy by ultrasound examination of the gestational sac at weeks 5-7.

NCT ID: NCT03666364 Completed - Infertility Clinical Trials

Magnetic Nanoparticle Sperm Separation for Teratozoospermia Male and Women Older Than 35 Years

Start date: September 17, 2018
Phase: N/A
Study type: Interventional

Women over 35 years old are likely to suffer from impaired oocyte repair capacity. Teratozoospermia is a condition reflects morphological affection of sperm. These spermatozoa would add an extra burden on the oocyte after ICSI. Whether selecting mature sperm by magnetic nanoparticle protocol would provide a more competent sperm to a likely affected oocyte would improve ICSI outcomes is the question of this research.

NCT ID: NCT03665103 Completed - Infertility Clinical Trials

Laser-assisted ICSI Versus Conventional ICSI

Start date: September 17, 2018
Phase: N/A
Study type: Interventional

Degeneration rate after ICSI is expectable but decreasing it is a goal. Laser-assisted ICSI can serve to decrease this degeneration rate.

NCT ID: NCT03663634 Completed - Infertility Clinical Trials

Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin B

ICSI-CB
Start date: September 16, 2018
Phase: N/A
Study type: Interventional

Vienna Consensus has identified 10% damage rate after ICSI as a competency value. Despite the highest quality embryologists doing ICSI, degeneration sometimes occurs due to oocyte factors such as the fragile membrane, etc. Cytochalasin B serves to facilitate spindle or pronuclear transfer procedures helping to reduce the damage rate with no harm reported. Using Cytochalasin B during ICSI could serve to rescue some oocytes from the degeneration allowing for more chances of viable zygotes,