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Endometriosis clinical trials

View clinical trials related to Endometriosis.

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NCT ID: NCT02100345 Completed - Bowel Endometriosis Clinical Trials

Conservative Treatment of Rectosigmoid Endometriosis Monitored by Transvaginal Ultrasound

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

Background: Endometriosis is a disease affecting 8-15 % of fertile women and is a cause of abdominal pain and suffering during women's menstrual periods. A subgroup of patients with DIE has an infiltration into the rectosigmoid bowel wall (4-37%). Knowledge of the growth pattern of rectosigmoid lesions related to subjective symptoms is mandatory in order to assess the need for follow-up with transvaginal ultrasound during medical treatment. Hypotheses: Symptoms will follow growth of rectosigmoid endometriosis. Material and methods: Two different cohorts of women, based on time of diagnosis of rectosigmoid endometriosis and treatment with hormonal intrauterine device or continuous oral contraceptives will receive a questionnaire and a transvaginal ultrasound scan (measuring size and volume) at inclusion, (6) and 12 months later. Perspectives: Patients treated conservatively may be followed by questionnaires, thereby reducing the need for time consuming clinical controls.

NCT ID: NCT02098668 Completed - Clinical trials for Polycystic Ovary Syndrome

Mathematical Model for the Human Menstrual Cycle, Endocrinological Diseases and Fertility Treatment-PAEON

PAEON
Start date: September 2013
Phase: N/A
Study type: Observational

Development of a bio-mathematical model of the human female cycle

NCT ID: NCT02093390 Completed - Prostate Cancer Clinical Trials

A Phase 1 Study to Evaluate the Effects of Fluconazole and Atorvastatin on the Pharmacokinetics of TAK-385 in Healthy Subjects

Start date: March 2014
Phase: Phase 1
Study type: Interventional

This is a nonrandomized, open-label, fixed-sequence, 2-arm study designed to assess the effect of multiple doses of fluconazole or atorvastatin on the single-dose pharmacokinetics of TAK-385 in healthy adult subjects.

NCT ID: NCT02091557 Completed - Endometriosis Clinical Trials

CA 125 and VAS Pain Score Changes to Diagnose Endometriosis

Start date: January 2011
Phase: N/A
Study type: Observational

To assess the diagnostic accuracy for the noninvasive detection of pelvic endometriosis of the combination of two simple parameters: modifications of serum CA 125 and VAS pain score following one dose of GnRH-analog (GnRH-a).

NCT ID: NCT02086279 Completed - Endometriosis Clinical Trials

AMH Levels Change During Treatment With GnRh Agonist

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

To evaluate the variation of AMH levels in women undergoing treatment with GnRHa, and to assess whether this variation correlates with changes in the antral and pre-antral follicle ultrasonographic count (AFC).

NCT ID: NCT02058212 Completed - Endometriosis Clinical Trials

Use of Antioxidant in Endometriotic Women to Improve Intracytoplasmic Sperm Injection (ICSI)

ROS
Start date: March 2013
Phase: Phase 2
Study type: Interventional

ROS plays an essential role in the pathogenesis of many reproductive processes. High follicular fluid ROS levels are associated with negative IVF outcomes. is plasma level of reactive oxygen species is affected by antioxidant treatment in endometriotic women?

NCT ID: NCT02047838 Completed - Surgery Clinical Trials

Second Laparoscopic Surgery for Recurrent Unilateral Endometriomas.

Start date: January 2007
Phase: N/A
Study type: Observational

This retrospective case-control study was performed in an Academic centre for the diagnosis and treatment of endometriosis. It included patients with recurrent unilateral endometriomas who were previously operated for the same condition (cases) and patients without recurrency who previously underwent surgery for unilateral endometrioma (controls). The primary outcome of the study was to assess the impact on ovarian reserve of second surgery for recurrent unilateral endometriomas. The evaluation of ovarian reserve was performed by assessing serum anti-mullerian hormone (AMH) level, serum follicle-stimulating hormone (FSH) level, 17-beta estradiol level and antral follicle count (AFC).

NCT ID: NCT02027142 Completed - Sleep Clinical Trials

Sleep Quality, Daytime Sleepiness and Insomnia in Patients With Endometriosis: a Case-control Study.

Start date: May 2012
Phase: N/A
Study type: Observational

This study included women referred to two academic centres for the diagnosis and treatment of endometriosis (cases) and women referred to our Institutions because of routine gynaecologic consultations (controls). In this age-matched case-control study, the aimdy was to assess quality of sleep, the average daytime sleepiness and insomnia in patients with endometriosis by using three different self-reported questionnaires.

NCT ID: NCT01982526 Completed - Surgery Clinical Trials

Role of Anti Mullerian Hormone for Ovarian Reserve Determination of Preoperative and Postoperative Endometrioma Patients

Start date: May 2012
Phase:
Study type: Observational [Patient Registry]

Ovarian reserve influenced by many factor but especially cysts like endometrioma. Anti mullerian hormone is recent marker for ovarian reserve. The investigators are searching ovarian reserve pre and post operatively by using antimullerian hormone of endometrioma patient who are operated for their cysts.

NCT ID: NCT01968694 Completed - Endometriosis Clinical Trials

Effects of Intravenous Lidocaine on Endometriosis Pain

Start date: December 2010
Phase: N/A
Study type: Interventional

We are doing this research study to find out if intravenous (in your vein, "IV") lidocaine can lessen pain from endometriosis. The U.S. Food and Drug Administration (FDA) has approved intravenous lidocaine to treat irregular heart beats, but the FDA has not approved intravenous lidocaine to treat pain from endometriosis. Intravenous lidocaine has been used for more than 25 years to treat different acute and chronic pain conditions but has not yet been studied for endometriosis pain. This is a cross-over trial over two months where one month you will receive the active medication (lidocaine) and one month you will receive the active placebo (diphenhydramine, commonly known as benadryl). We will compare the effect on pain from endometriosis of lidocaine to active placebo.