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Embryo Implantation clinical trials

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NCT ID: NCT05555121 Active, not recruiting - Fertility Issues Clinical Trials

Rescue Progesterone Supplementation During Frozen Embryo Transfer

P4R
Start date: December 1, 2022
Phase: Phase 2
Study type: Interventional

Endometrin is a progesterone supplement prescribed during in vitro fertilization (IVF) for preparation for embryo transfer. The usual dose of Endometrin is 100 mg two to three times per day in the form of an effervescent tablet to be inserted vaginally. The purpose of this research project is to evaluate the dose response of the Endometrin when determined based on the blood level of progesterone on the day of the FET. According to the literature, a predefined level of progesterone in the blood should be reached in order to have favorable conditions for pregnancy. The hypothesis being that a woman with low progesterone levels would benefit from a dose of Endometrin of 600 mg (200 mg 3x/day) to decrease the risk of miscarriage and improve the chances of pregnancy. Women with adequate progesterone levels according to the literature, would continue with the standard dose of progesterone prescribed at clinique ovo which is 300 mg (100 mg 3x/day). PIBF (Progesterone Induced Blocking Factor) levels, a protein found in the blood that could also predict pregnancy outcomes in women using IVF will also be looked at.

NCT ID: NCT04855383 Completed - Embryo Implantation Clinical Trials

Intramuscular Injection of Human Chorionic Gonadotropin in Frozen Embryo Transfer Cycles

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

This study is a randomized controlled clinical trial to compare the pregnancy outcomes of infertile women with frozen embryo transfer. The study population in frozen embryo transfer cycles receive three doses of human chorionic gonadotropin (HCG) to recognize the effectiveness of HCG on pregnancy outcomes in Reproductive Biomedicine Research Center, Royan institute, Tehran Iran.

NCT ID: NCT04744844 Terminated - Embryo Implantation Clinical Trials

DNA Amplification in Blastocoel Fluid

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Introduction: Although innovative procedural changes in frozen embryo transfer (FET) cycles have increased the implantation rate of blastocysts transferred significantly, blastocyst selection remains a significant limiting factor in implantation outcomes. To improve implantation rates requires conventional microscopic blastocyst morphology scoring/selection technique to be replaced by an enhanced blastocyst selection technique or for the conventional morphology selection technique to be strengthened by novel supplementary selection techniques. Blastocoel fluid biopsy with DNA amplification is a minimally invasive (mi) technique that may supplement a blastocyst morphology score variables with a genetic variable. Objective: In the present randomized controlled trial (RCT), DNA amplification in blastocoel fluid biopsies (BF-biopsy) will be investigated as a supplementary measure to select blastocysts for transfer in conjunction with blastocyst morphology scores. The objective will be to develop a minimally invasive blastocyst selection technique, which will improve selection and increase clinical implantations, while not increasing costs. Materials and Methods: A single IVF centre double-blind randomised controlled trial, with patients recruited having female age 18 to 35 years from infertile patients presenting for freeze-all-IVF treatment. Enrolled patients (N = 500) with ≥five 2PN zygotes after ICSI will be randomised (1:1) to the two arms of the trial (i.e., test and control arm). In the test arm, 3 blastocysts will undergo blastocoel fluid biopsy (BF-biopsy) and whole-genomic amplification. Single blastocysts with no DNA amplification will be transferred in FETs of the test arm and single top-scoring blastocysts will be transferred in FETs of the control arm. The primary outcome measure of the trial will be clinical implantation (i.e., gestational sac with fetal heartbeat). Results: The clinical implantation outcomes of FETs in which score-selected single blastocyst with no DNA amplification and score-selected single blastocysts were transferred will be compared.

NCT ID: NCT04721522 Recruiting - ART Clinical Trials

The Impact of Endometrial Compaction on Assisted Reproductive Technology Outcome

Start date: January 29, 2021
Phase:
Study type: Observational

Absence of endometrial compaction on the day of ET has adverse effects on success of ART outcome.

NCT ID: NCT04159649 Recruiting - EMBRYO IMPLANTATION Clinical Trials

The Outcomes of ICSI Cycles With and Without Letrozole

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

A variety of genes working together with ovarian hormones conducts and precisely control the process of endometrial receptivity and implantation. Leukemia inhibitory factor and αvβ3 integrin are two markers of implantation with at most importance. Reports have emphasized that these important biomarkers have a great role during the process of embryonic implantation. αvβ3 integrin is one of the adhesion molecules which has a critical role in blastocyst apposition and attachment. Many studies have demonstrated that abnormal expression of αvβ3 integrin is associated with poor reproductive outcomes. Other studies haven't found a strong relation between αvβ3 integrin expression and reproductive outcomes Letrozole is an aromatase inhibitor which has been used in controlled ovarian stimulation especially in women with PCOS . Data suggests that letrozole addition to gonadotropins during ovarian stimulation protocols improve the response of the ovaries to FSH in low responders and increase the number of preovulatory follicles without adversely affect the outcomes. Letrozole is used as an adjuvant therapy in ovarian stimulation protocols. So this study aims to evaluate whether the use of letrozole in combination with gonadotropins and GnRH antagonist is superior to gonadotropins and antagonist alone in women undergoing ICSI treatment. Furthermore, both αvβ3 integrin and leukemia inhibitory factor are important markers of endometrial receptivity and implantation. Therefore, this study aims to assess the correlation between mid-luteal gene expression of both αvβ3 integrin and leukemia inhibitory factor and the clinical outcomes of antagonist cycles with or without letrozole.

NCT ID: NCT04077970 Completed - Embryo Implantation Clinical Trials

Intrauterine Flushing With Follicular Fluid Plus Granulosa Cells

Start date: November 1, 2018
Phase: Phase 3
Study type: Interventional

One hundred forty patients with male factor infertility are randomized into two groups. In the study group, flushing the endometrial cavity with 2ml of clear follicular fluid with granulose cells will be performed using an IUI catheter after ovum pick-up While in the control group, no flushing of the endometrial cavity with FF is done. The implantation rates and pregnancy rates in both groups will be assessed.

NCT ID: NCT04003337 Recruiting - Embryo Implantation Clinical Trials

Selection of the Embryo to Transfer by Morphokinetics vs. Morphological Evaluation.

EmbryoSEL
Start date: January 26, 2017
Phase: N/A
Study type: Interventional

Our study intends to demonstrate that the selection of an embryo to transfer it at the sage of blastocyst through morphokinetics (analysis of embryos depending not only in their morphology —that is, the aspect of the embryo—, but also based on times of cell division) during the use of time-lapse (Embryoscope®) may have a better impact in clinical results, as selection is not performed in mere morphological evolution (visual aspect of the embryo) of the embryos.

NCT ID: NCT03485235 Completed - Embryo Implantation Clinical Trials

Effect of Dilatation and Curettage on the Endometrial Receptivity

Start date: March 31, 2018
Phase: N/A
Study type: Interventional

Effect of dilatation and curettage on the endometrial receptivity and pregnancy outcome in patients with recurrent implantation failure

NCT ID: NCT03128970 Completed - Embryo Implantation Clinical Trials

Synchronizing Blastocyst in Frozen Embryo Transfer

Start date: April 21, 2017
Phase: N/A
Study type: Interventional

The aim of the present study is to determine if implantation rate could be increased in women undergoing frozen embryo transfer cycles in case of adjusting their embryo development at hatching stage.

NCT ID: NCT03108157 Completed - EMBRYO IMPLANTATION Clinical Trials

Endometrial Scratch Effect on Pregnancy Rates in Patients Undergoing Egg-donation IVF

Start date: January 12, 2017
Phase: N/A
Study type: Interventional

Clinical trial about the effect of endometrial scratch on pregnancy rates in patients undergoing a treatment with in-vitro fertilization with donor eggs, when doing the endometrial biopsy during the cycle prior to the embryo transfer.