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Female Reproductive Problem clinical trials

View clinical trials related to Female Reproductive Problem.

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NCT ID: NCT03617354 Completed - Clinical trials for Female Reproductive Problem

The Implementation of MinimAlly Invasive Hysterectomy Trial

IMAGINE
Start date: March 29, 2017
Phase:
Study type: Observational

Removal of the uterus (hysterectomy) is the most commonly performed major gynaecological procedure in women. Obstetricians and gynaecologist (O&G) surgeons conduct the majority of hysterectomies. Surgical approaches to removal of the uterus include laparoscopic hysterectomy, vaginal hysterectomy with or without laparoscopic assistance and open hysterectomy through an abdominal incision. It is widely accepted that laparoscopic hysterectomy and vaginal hysterectomy are less invasive procedures, cause fewer surgical complications, less postoperative pain, require a shorter hospital stay and are associated with quicker recovery than abdominal hysterectomy. In Australia and despite the evidence, Total Abdominal Hysterectomy (TAH) rates are unreasonably high (~40%) and only 13% of all hysterectomies are done via Total Laparoscopic Hysterectomy (TLH) in Australia. This study aims to implement and evaluate a training program in TLH for gynaecologists. The potential benefits to the community are: - A reduction in the incidence of overall surgical adverse events in patients receiving a hysterectomy - A reduction in the length of hospital stay for patients requiring a hysterectomy - A reduction in the direct hospital costs for hysterectomy

NCT ID: NCT02644304 Recruiting - Clinical trials for Female Reproductive Problem

Clomiphene Citrate Plus Cabergoline in Treatment of Polycystic Ovary Syndrome

Start date: May 2015
Phase: Phase 2
Study type: Interventional

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder of reproductive aged women and affects approximately 5-12 % of the female population. In 2003 in Rotterdam , Rotterdam diagnostic criteria were redefined PCOS as affected individuals must have two out of the following three criteria: 1. Oligo- and/or anovulation, (ovulation occurs less than once every 35 days). 2. Hyperandrogenism, clinical signs include hirsutism, acne, alopecia, and frank virilization, while chemical indicators include raised concentrations of total testosterone and androstenedione , and elevated free androgen index. 3. Polycystic ovaries on sonographic examination, presence of 12 or more follicles in either ovary measuring 2-9 mm in diameter, increased ovarian volume more than 10 cm3 and/or increase in stromal echogenicity. Clearly, according to the Rotterdam diagnostic criteria, the majority of women with PCOS can be diagnosed without the need of laboratory examinations. Clomiphene citrate (CC) is still the first-line medication for the induction of ovulation. It is an anti-estrogenic compound made up of two isomers, enclomiphene and zuclomiphene; the latter being the more potent of the two. It is a non-steroidal compound closely resembling estrogen. CC acts by blocking estrogen receptors, particularly in the hypothalamus, thereby signaling a lack of circulating estrogens and inducing a change in the pulsatile release of gonadotrophin-releasing hormone (GnRH). This induces release of follicle stimulating hormone from the anterior pituitary and is often enough to set the cycle of events leading to ovulation into motion. Cabergoline, ergot-derived dopamine agonists with a very long half life, is an effective prolactin suppressor. Cabergoline oral administration contains a weekly dose of 0.5 - 3 mg, which could be increased, if needed, to twice a week. This medicine has slight dopamine agonistic side effects, headache being the most common one. Treatment in the very beginning should start with a partial dose (half a pill) at bedtime with a small amount of food. Low incidence of side effects and its weekly dose has made Cabergoline a choice drug for treatment of related diseases.

NCT ID: NCT02377219 Terminated - Clinical trials for Female Reproductive Problem

Bisphenol A Exposure, Ovarian Function and Assisted Reproductive Technology Outcome.

FIVPHENOL
Start date: October 2014
Phase: N/A
Study type: Interventional

Our goal is to prospect the relationships between Bisphenol A (BPA) exposure (measured as its free and conjugated forms in blood and urine) and embryo implantation rate (measured as the ratio between the number of gestational sacs and the number of transferred embryos) after assisted reproductive technology. In order to reduce the confusion factors, the population study is limited to young women (aged 28 to 34), with regular menstrual cycles and without any medical event that could affect the implantation process

NCT ID: NCT02249390 Completed - Clinical trials for Female Reproductive Problem

Assisted Reproductive Technology Survey (ART Survey)

ART
Start date: September 2014
Phase:
Study type: Observational

The purpose of the study is to collate local information to better understand the motivations, accessibility and frequency of assisted reproductive technology (ART) use in the community.

NCT ID: NCT02213627 Unknown status - Infertility Clinical Trials

Use of Corifolitropin Alfa in Oocyte Donors

Start date: October 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if corifollitropin alfa (long-term gonadotropin administration) is effective in a controlled ovarian stimulation protocol in oocyte donors compared to daily gonadotropin administration (recombinant FSH or HP-hMG)