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Pregnancy Rate clinical trials

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NCT ID: NCT05721495 Completed - Pregnancy Rate Clinical Trials

Deferred Embryo Transfer in an In Vitro Program With Single Embryo Transfer Policy

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Single embryo transfer decreases the multiple pregnancy rate and its complications. However, studies are needed to help increase the effectiveness of this technique to increase its use, which undoubtedly improves the safety of our patients. Objectives: To assess the results of IVF / ICSI cycles with single embryo transfer, in terms of both pregnancy and live birth rates, comparing a group of patients in which an elective delayed cryotransfer of an embryo without fresh transfer is performed (experimental group ), with patients in whom a fresh embryo is transferred electively. Methodology: A prospective randomized clinical trial with two arms in parallel, not blinded, including 138 couples using an IVF / ICSI cycle at the Reproduction Unit of the Hospital Universitario Virgen de las Nieves de Granada. The inclusion criteria classify them as having a good reproductive prognosis, and the patients will follow an ovulation treatment protocol with GnRH agonists or antagonists. Couples will undergo an IVF / ICSI cycle, randomly assigned to: - Group I (experimental): fresh transfer is not performed, the best quality embryo is cryopreserved. Elective transfer in a later cycle of the cryopreserved embryo. - Group II (control): fresh transfer of the best quality embryo.

NCT ID: NCT05467852 Not yet recruiting - Pregnancy Rate Clinical Trials

Didroxyprogesterone Promotes Natural Pregnancy in Infertile Patients With Endometriosis

Start date: December 10, 2022
Phase: Phase 3
Study type: Interventional

Endometriosis (EM) is an important cause of infertility in women of childbearing age. Laparoscopic surgery is the treatment of EM Related infertility is an important method. However, excluding other infertility factors, the natural pregnancy rate of EM patients one year after operation is still significantly lower than that of normal couples. At the same time, the high recurrence rate of EM often requires drugs to inhibit ovulation after operation, which forms a paradox with the demand for fertility. One year after operation is the "golden period" of natural pregnancy. Whether to treat the recurrence of EM without affecting or even promoting fertility is a key problem to be solved in clinic. Didroxyprogesterone is the closest natural progesterone. It is widely used in luteal support and treatment of threatened abortion. It does not affect ovulation and is harmless to embryos. In recent years, clinical studies have found that it is helpful to the natural pregnancy of patients with EM after operation, and is beneficial to improve pain symptoms and reduce the recurrence rate. Basic studies have also confirmed the inhibitory effect of didroxyprogesterone on em. However, the existing studies with small sample size are not enough to draw a convincing conclusion that didroxyprogesterone promotes the pregnancy rate after em, and there is a lack of Chinese data. This study intends to use a multicenter, prospective, open, randomized controlled clinical trial design to explore the value of didroxyprogesterone in the treatment of EM related infertility patients, so as to provide direct evidence for improving the postoperative natural pregnancy rate of EM patients.

NCT ID: NCT05173038 Not yet recruiting - Pregnancy Rate Clinical Trials

Second Ejaculate and IUI

Start date: May 1, 2022
Phase:
Study type: Observational [Patient Registry]

The WHO operation specification requires men to maintain a 2-7-day ejaculation abstinence period before semen examination, but it does not mention the possibility of obtaining a second sample immediately after the first sample for evaluation, and the significance of the evaluation of the second sample for fertility. There is a certain fluctuation level in sperm concentration detection. Patients with normal previous detection may have lower sperm concentration on the day of IUI, resulting in the trouble of canceling IUI. It is not clear whether patients with previous oligospermia can obtain more sperm with better vitality and improve the success rate of IUI by taking sperm again. Some retrospective studies found that when the semen abstinence period of oligozoospermia men was as short as 40 minutes, the changes of sperm motility and sperm concentration were significantly improved, but there was no difference in the conclusions of other studies. A small number of assisted reproduction studies found that IUI with samples obtained during abstinence period of less than 2 days could obtain better pregnancy rate. However, the quality and sample size of these retrospective studies are limited, the repeatability is not good enough, and the conclusions are still controversial. We designed a randomized controlled study. Semen examination was performed after sperm extraction. If the sperm concentration after treatment was less than 10m, the subjects were included in the study. They were randomly divided into two groups. Group 1 received IUI for pregnancy assistance directly, and group 2 received IUI for pregnancy assistance 1 hour after the first sperm extraction. The two semen were mixed and treated. 205 subjects were included in the two groups. We tried to explore whether secondary sperm extraction in patients with low IUI concentration can improve the success rate of IUI pregnancy.

NCT ID: NCT04619914 Completed - Pregnancy Rate Clinical Trials

the Effect of Clomiphene Citrate Plus Estradiol Valerate Versus Letrozole on Endometrial Thickness and Pregnancy Rate in Infertile Women

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

The present randomized double blind study has been carried out in Gynecology and Obstetrics Department, Faculty of Medicine, Zagazig university on 70 women were previously received clomiphene citrate alone as management of infertile anovulatory PCOS women, but giving improper endometrial thickness < 7mm during the period from March 2019 to September 2019

NCT ID: NCT04500743 Completed - Endometriosis Clinical Trials

Role of Suppression of Endometriosis With Progestins Before IVF-ET

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

This study aimed to assess the role of Dienogest pretreatment for endometriosis suppression as compared to Gonadotropin-releasing hormone agonist (GnRHa) in patients with endometriosis pursuing IVF treatment.

NCT ID: NCT04389203 Recruiting - Pregnancy Rate Clinical Trials

Pregnancy Rate After Unilateral Tubal Disconnection

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

Unilateral disconnection of one tube that had hydrosalpinx

NCT ID: NCT03579550 Enrolling by invitation - Ectopic Pregnancy Clinical Trials

Hysteroscopic Metroplasty in Unexplained Infertile Women With Dysmorphic Uterus

COH/IUI
Start date: June 8, 2018
Phase: N/A
Study type: Interventional

The correlation between dysmorphic uterus and infertility still remains enigmatic. We aim to evaluate the reproductive outcomes of metroplasty via office hysteroscopy in unexplained infertile women with dysmorphic uterus with comparing a group of unexplained infertile women performing 6 months spontaneous cycles plus 3 cycles controlled ovarian hyperstimulation and intrauterine insemination by randomized trial.

NCT ID: NCT02809989 Completed - Pregnancy Rate Clinical Trials

A Study to Evaluate the Effect of Ovaleap® on the Pregnancy Rate and Clinical Effects as Well as the User-friendliness of the Ovaleap®-Pen.

Start date: March 31, 2016
Phase:
Study type: Observational

The aim of this non-interventional study is to extend the knowledge on effectiveness of Ovaleap® (number of oocytes and pregnancy rate) during routine IVF- or ICSI-treatment using a Gonadotropin-releasing hormone (GnRH) antagonist protocol in a large number of patients.

NCT ID: NCT02099916 Not yet recruiting - Clinical trials for Diminished Ovarian Reserve

Administration of DHEA in Patients With Poor Response to Ovarian Stimulation for IVF

DHEA
Start date: October 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Poor responders to ovarian stimulation represents one of the most frustrating problems in reproductive medicine. The investigators hypothesize that ovarian response of those patients could improve by treating these patients with 25 mg DHEA tid for 12 weeks prior to stimulation.

NCT ID: NCT01933126 Recruiting - Pregnancy Rate Clinical Trials

Intrauterine Injection of HCG and Implantation Rate

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

The study aims to examine the effect of intrauterine injection of HCG on pregnany rate in women undergoing IVF treatment.