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Infertility clinical trials

View clinical trials related to Infertility.

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NCT ID: NCT03012412 Completed - Infertility Clinical Trials

Mindfulness Based Program for Infertility

MBPI
Start date: May 2009
Phase: N/A
Study type: Interventional

The current study aims to test the efficacy a mindfulness based intervention for women facing fertility problems - the Mindfulness Based Program for Infertility (MBPI). MBPI comprises 10 weekly group sessions of approximately 2 hours each, run in small groups of 10-15 women. The main goal of MBPI intervention is to reduce depressive and anxiety symptoms and promote infertility self-efficacy and acceptance and mindfulness skills. The MBPI is intended to develop willingness/acceptance through a process of contacting the present moment and be in touch with the unfolding experience in an open and non-judgmental way, particularly infertility-related experiences.

NCT ID: NCT03006523 Completed - Infertility Clinical Trials

0.2 ml vs. 0.5 Inseminated Volume in Donor Intrauterine Insemination Cycles: A Prospective RCT

Start date: March 2013
Phase: N/A
Study type: Interventional

To prospectively determine the most appropriate inseminated volume in donor IUI cycles. It is hypothesized that if the procedure is performed with 0.5 mL instead of 0.2, higher clinical pregnancy rates will be achieved by promoting higher sperm densities in the fallopian tubes at the time of ovulation by decreasing the amount of sperm cells lost during preparation and handling.

NCT ID: NCT03001648 Completed - Infertility Clinical Trials

Cumulative Live Birth Rates in Patients With Repeated Implantation Failure (RIF) Undergoing Preimplantation Genetic Screening (PGS )

Start date: January 2014
Phase: N/A
Study type: Observational

This is a single centre retrospective study in repeated implantation failure patients: < 39 years old, at least 4 D3 good quality embryos or 2 good quality blastocysts transferred without implantation, absence of known causes of implantation failures (uterine malformation, thrombophilia, severe male factor, uncontrolled thyroid disfunction, autoimmune disease). Patients scheduled for PGS underwent one or more stimulation cycles (oocyte or blastocyst banking) in order to maximize chances of embryo transfer. PGS cycles are analyzed globally. Aditionally, PGS cycles with a single stimulation cycle are analyzed in comparison to standard IVF cycles.

NCT ID: NCT02994550 Completed - Sub-Fertility Clinical Trials

Influence of FSH/LH Ratio in Controlled Ovarian Stimulation

Start date: January 2017
Phase: Early Phase 1
Study type: Interventional

The aim of this study is to compare different FSH/LH ratios in controlled ovarian stimulation

NCT ID: NCT02990013 Completed - Clinical trials for Cleaning Product Causing Toxic Effect

AvenovaTM as a Sterile Skin Preparation Agent

Start date: December 1, 2018
Phase: Early Phase 1
Study type: Interventional

Aim 1: To determine in vivo capability of AvenovaTM against common cutaneous microbial biome on human skin Aim 2: To compare to povidone-iodine 5% solution, 4% chlorhexidine and isopropyl alcohol against AvenovaTM as a sterile skin agent

NCT ID: NCT02988544 Completed - Clinical trials for Infertility Assisted Reproductive Technology

Artificial Shrinkage of Fresh Blastocysts

BlastoCollapse
Start date: May 20, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to determine if collapsing an embryo (or making it fold compactly by taking away its fluid) before the transfer in the uterine cavity improves pregnancy rates in assisted reproductive technology (ART). Women coming to our ART center will be randomized in two groups : the collapsing group and a control group. Pregnancy rates will be compared in the two groups. A biomarker (cell free DNA) will also be determined in each group and correlated to pregnancy occurrence.

NCT ID: NCT02987023 Completed - Infertility, Female Clinical Trials

Uterus Transplantation From Live Donors With Robotic Assisted Surgery - Gothenburg II

UTX-robot
Start date: November 2016
Phase:
Study type: Observational [Patient Registry]

The study is a follow up of NCT01844362. Uterus transplantation will be performed from live donors to patients with uterine factor infertility. If will be performed before transplantation. Organ procurement from the donor will be performed by robotic assisted laparoscopy. Transplantation will be by laparotomy. Embryo transfer will be done 10-12 months after transplantation. After birth of 1-3 children the uterus will be removed by hysterectomy,

NCT ID: NCT02984774 Completed - Infertility, Female Clinical Trials

Assessment of Telomerase Activity in Endometrial Tissue and Serum in Endometriosis Patients

Start date: June 2014
Phase: N/A
Study type: Interventional

The goal of the study was the detection of telomerase activity in eutopic, ectopic endometrial tissue and in peripheral blood and finding the correlation between the telomerase activity and clinic findings. With these results, confirmation of the hypothesis regarding the endometriosis pathogenesis and endometriosis-related infertility was aimed.

NCT ID: NCT02961907 Completed - Infertility Clinical Trials

Pathway Taking Into Account PeriConceptional Environment for Infertile Couple

PEPCI
Start date: January 22, 2018
Phase: N/A
Study type: Interventional

Infertility is defined as the inability to conceive after 12 months of unprotected intercourse, It affects approximately one in six couples pregnancy. Many lifestyle factors of the couple's pre and peri-conceptional environment (weight, diet, alcohol, tobacco, coffee, drugs, exercise, stress, sleep, pollution...) are risk factors for infertility. Weight gain, in both members of the couple, is associated with an increased risk of Assisted Reproduction Technology (ART) failure and adverse pregnancy outcome, while healthy lifestyle makes the risk of infertility three times less likely to happen. Idiopathic infertility may greatly benefit from lifestyle factors optimization.

NCT ID: NCT02946684 Completed - Infertility Clinical Trials

Effect of Addition of Aromatase Inhibitor to Ovarian Stimulation Therapy in IVF Treatment

RIOT-A
Start date: February 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

This project seeks to determine whether estradiol suppression achieved with adjuvant treatment with an aromatase inhibitor improves end-follicular and midluteal phase parameters during IVF. 128 patients will be randomized to either placebo or active treatment.