Clinical Trials Logo

Ovulation Disorder clinical trials

View clinical trials related to Ovulation Disorder.

Filter by:

NCT ID: NCT06433453 Recruiting - Ovulation Disorder Clinical Trials

Three Dimensional Ultrasonographic Detection of Human Ovulation

Start date: April 22, 2024
Phase: Phase 4
Study type: Interventional

The research aims to compare diagnosis of ovulation and anovulation in 2D and 3D ultrasonography.

NCT ID: NCT06292806 Not yet recruiting - Infertility, Female Clinical Trials

Inhibin B/AFC Ratio for Ovarian Response

Start date: March 1, 2024
Phase:
Study type: Observational [Patient Registry]

Ovarian response to gonadotropin stimulation plays a major role in the success of in vitro fertilization (IVF). Anti-müllerian hormone (AMH), inhibin B, and antral follicle count (AFC) are ovarian reserve markers and also predictors of the ovarian response, as they correlate with the number of oocytes retrieved. Ovarian responsiveness can also be assessed through the Follicular Output Rate (FORT), which evaluates the proportion of follicles that developed during stimulation by the ratio of PFC (preovulatory follicle count) to AFC. FORT highlights that some follicles do not respond to the FSH; therefore, this project proposes an endocrinological approach to this issue by relating AFC to inhibin B and AMH ㅡ hormones produced by granulosa cells, but at different stages of folliculogenesis and with endocrine and paracrine functions, respectively. The inhibin B/AFC and AMH/AFC ratios correlated with FORT and the number of oocytes retrieved may help elucidate the mechanisms involved in follicular responsiveness. A prospective cohort study will be conducted with patients of the Insemine Center for Human Reproduction. Antral follicle count and AMH measurement will be performed before IVF cycle initiation, and inhibin B measurement will be carried out on a blood sample collected on the fifth day of ovarian stimulation. The primary outcomes will be the Follicular Output Rate (FORT) and the number of oocytes retrieved. Secondary outcomes include the number of metaphase II oocytes, oocyte quality, fertilization rate and embryo quality.

NCT ID: NCT05211583 Recruiting - Ovulation Disorder Clinical Trials

Serial Progesterone Level Measurements During the Menstrual Cycle in Subfertile Women

Start date: December 10, 2021
Phase:
Study type: Observational

Ovulatory dysfunction is identified in 15% of all infertile couples and it accounts for 40% of female infertility. Ovulatory dysfunction may be more subtle in women with regular menses. Detecting the day of ovulation is necessary for optimizing natural conception, diagnosis of cycle disturbances and also timing for embryo transfer in natural cycle frozen-thawed embryo transfers. In order to diagnose ovulatory dysfunction, ovulation physiology and change of reproductive hormones during the menstrual cycle should be understood. In the present study we aimed to evaluate serial serum hormonal cut-off levels referenced to ovulation in subfertile women with regular menses.

NCT ID: NCT04979377 Recruiting - Type 1 Diabetes Clinical Trials

Prevalence of Hyperandrogenism in Type 1 Diabetes

Start date: March 9, 2020
Phase:
Study type: Observational

The investigators aim to estimate the prevalence of functional ovarian hyperandrogenism [idiopathic hyperandrogenism, idiopatic hirsutism, and polycystic ovary syndrome (PCOS)] in adult patients with type 1 diabetes (T1DM) in an observational cross-sectional study. Study population is comprised of premenopausal adult women with a diagnosis of T1DM, consecutively recruited from a Diabetes outpatient clinic at a tertiary hospital in Spain, Europe.

NCT ID: NCT04942457 Completed - Fertility Disorders Clinical Trials

Feasibility and Safety of Fasting in Fertility Treatment

KiWuA
Start date: January 10, 2022
Phase: N/A
Study type: Interventional

This exploratory study investigates fasting as a potential supportive therapy in infertility treatment for women suffering from infertility

NCT ID: NCT04210765 Completed - Clinical trials for Unexplained Infertility

Incremental Clomiphene Citrate Doses in Successive Cycles and FSH, LH and Steroid Hormone Levels

Start date: August 2, 2019
Phase: Phase 4
Study type: Interventional

This study was planned to assess the initial and endogenous FSH, LH and steroid responses to incremental CC doses in successive ovulation induction cycles to treat anovulation in patients with unexplained infertility.

NCT ID: NCT04075149 Recruiting - Clinical trials for Polycystic Ovary Syndrome

Does Treatment of Androgen Excess Using Spironolactone Improve Ovulatory Rates in Girls With Androgen Excess?

CBS009
Start date: December 18, 2019
Phase: Early Phase 1
Study type: Interventional

Adolescent girls with androgen excess have a higher rate of irregular periods and decreased ovulation rates compared to normal girls, and are considered at-risk for developing polycystic ovary syndrome (PCOS). This pilot study will look at whether giving spironolactone might improve ovulation rates in girls with androgen excess, ages 13-19. If this is true, spironolactone treatment to young girls might prevent PCOS from developing and avoid future infertility.

NCT ID: NCT04002635 Withdrawn - Clinical trials for Polycystic Ovary Syndrome

Letrozole for Frozen Embryo Transfer (FET) in Patients With Polycystic Ovary Syndrome (PCOS)

LEFT
Start date: December 1, 2020
Phase: Phase 4
Study type: Interventional

To offer patients with oligomenorrhoea or amenorrhoea an alternative to frozen embryo transfer in an artificial cycle, endometrial preparation using letrozole may be a valuable option. Letrozole, a potent, reversible nonsteroidal aromatase inhibitor with relatively short half-life, can successfully induce ovulation without any adverse anti-estrogenic effects and thus without affecting the endometrium. The use of letrozole typically results in monofollicular growth and this reduces the effect of supraphysiological levels of estrogen on the endometrium and embryo. The purpose of this study is to compare a frozen-thawed embryo transfer in an artificial cycle with a letrozole-induced ovulatory cycle, specifically in PCOS patients. The primary outcome is early pregnancy loss.

NCT ID: NCT03989024 Not yet recruiting - Infertility Clinical Trials

Pulsatile Gonadotropin-releasing Hormone for Infertility in Non-obese Patients With Polycystic Ovary Syndrome

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

Polycystic ovary syndrome (PCOS) patients are often accompanied by infertility. Non-obese PCOS infertility is more difficult to treat than obese PCOS. The study included non-obese PCOS patients who had not recovered from regular menstruation after six months of metformin treatment. Half of the patients were treated with clomiphene for ovulation induction and half with GnRH pulse therapy.

NCT ID: NCT03924453 Completed - Ovulation Disorder Clinical Trials

Usability Study of the Pearl Fertility Tracking Device

Start date: December 1, 2017
Phase:
Study type: Observational

This mobile application measures the level of certain hormones in the urine of a woman and is used to help pinpoint when the woman is/was most likely to get pregnant during her menstrual cycle.