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Menstruation Disturbances clinical trials

View clinical trials related to Menstruation Disturbances.

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NCT ID: NCT03673995 Completed - Clinical trials for Polycystic Ovary Syndrome

Myoinositol Plus L-tyrosine, Selenium and Chromium in PCOS

Start date: May 2, 2017
Phase: N/A
Study type: Interventional

PCOS patients were treated every day, with one sachet containing 2000 mg myo-inositol, 500 mg L-tyrosine, 40 mcg chromium picolinate, 55 mcg selenium, 200 mcg folic acid. All patients underwent, before starting the therapy, after 3 months and 6 months, hormonal evaluation , hirsutism scoring and ovulation assesment. Most of them during the treatment improved their symptoms.

NCT ID: NCT03652987 Suspended - Obesity Clinical Trials

Endocrine and Menstrual Disturbances in Women With Polycystic Ovary Syndrome (PCOS)

EMDPCOS
Start date: September 5, 2018
Phase:
Study type: Observational [Patient Registry]

Polycystic ovary syndrome (PCOS) is a common endocrine disorder in reproductive age women, which causes disordered follicle growth and ovulation resulting in infertility. In addition women with PCOS have hyperandrogenemia and a dysregulated hormonal profile, resulting in altered feedback on the hypothalamic-pituitary-gonadal (HPG) axis. Obesity, insulin resistance, vitamin D (VD) deficiency and ageing worsen the symptoms. The gonadotrophins - follicle stimulating hormone (FSH) & luteinising hormone (LH), along with the pregnancy hormone human chorionic gonadotrophin (hCG) have structural similarities. The altered levels of FSH and LH in women with PCOS cause production of hCG from the brain leading to false positive pregnancy tests. Part one of this project will involve the investigation of this over-production of hCG in urine and serum of women with PCOS to develop suitable ovulation and pregnancy test kits, in collaboration with Swiss Precision Diagnostics (SPD). In Part two of the project, we would like to see if intervention with VD supplementation and/or using myo-inositol supplement compared with metformin (insulin sensitiser), improves prediabetes, distribution of fat/water content, weight loss and menstrual cyclicity in women with PCOS. We aim to correlate these interventions with particular serum & urine markers to develop better diagnostic tools.

NCT ID: NCT03579303 Recruiting - Clinical trials for Polycystic Ovary Syndrome

Homoeopathy and Yoga in the Treatment of Menstrual Disorders in Females With Polycystic Ovarian Syndrome

Start date: October 2018
Phase: N/A
Study type: Interventional

This study is undertaken to compare effectiveness of homoeopathic treatment versus integrated approach of homoeopathy and yoga in the treatment of menstrual disorders in females with Polycystic ovarian syndrome.

NCT ID: NCT03547453 Completed - Clinical trials for Overweight and Obesity

Ovarian Ultrasonography for the Clinical Evaluation of Polycystic Ovary Syndrome

Start date: June 4, 2018
Phase:
Study type: Observational

The investigators would like to determine how aspects of adiposity and age influence ultrasound features of the ovaries which are used to diagnose polycystic ovarian syndrome (PCOS). The study will also compare anti-Müllerian hormone (AMH) levels against ultrasound features of the ovary to predict PCOS.

NCT ID: NCT02857972 Completed - Clinical trials for Other Menstruation Disorders

Proof Of Concept Menstrual Hygiene Product-Wondaleaf®

Start date: May 2016
Phase: N/A
Study type: Interventional

General objective: To assess the preference and performance in terms of satisfaction and acceptability as well as safety profile of a novel innovative design of menstrual hygiene device (Wondaleaf®) during the night for menstruating women by comparing it to prior experience of the usual hygienic product for menstrual control, i.e. sanitary pads. Specific objectives: - To determine the preference of participants between Wondaleaf® and usual sanitary pads as a night use menstrual hygiene product. - To determine the satisfaction of participants towards Wondaleaf® and usual sanitary pads as a night use menstrual hygiene product. - To determine the acceptability of participants towards Wondaleaf® as a night use menstrual hygiene product. - To determine the safety profile of the Wondaleaf®.

NCT ID: NCT02486757 Completed - Clinical trials for Menstruation Disturbances

Investigation of Female Reproductive Hormone Dynamics During Adolescence

Start date: April 2015
Phase: Early Phase 1
Study type: Interventional

Irregular menstrual cycles are common in girls for several years after their first menstrual period. The cause of abnormal menstrual cycles during this time is not well-understood. The purpose of this study is to: 1) monitor girls during a menstrual cycle (with blood and urine sampling and serial pelvic ultrasounds) to identify those girls who do not ovulate (release of an egg from the ovary), and 2) determine whether cycles can be corrected by treating girls with a short course of low-dose estrogen and progesterone.

NCT ID: NCT02092558 Completed - Clinical trials for System and Hematuria.

Evaluation of Immunological Disorders of T Lymphocytes and Endocrinological Disorders as Pathogen Factors in Patients With Metaplasia of Urinary Bladder

Start date: January 2005
Phase: N/A
Study type: Observational

Background: Squamous metaplasia refers to the pathological transformation of the urothelium leading to non-keratinised stratified squamous metaplasia (N-KSM). Objective: To present the investigators experiences in the diagnosis and treatment of N-KSM of the urinary bladder in children.

NCT ID: NCT02070692 Completed - Clinical trials for Menstruation Disturbances

Tamoxifen for the Treatment of Unfavorable Bleeding in Contraceptive Implant Users

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

The purpose of this study is to study whether a drug called tamoxifen can reduce vaginal bleeding in women who are using the Etonogestrel contraceptive implant.

NCT ID: NCT02035930 Completed - Clinical trials for Abnormal Menstrual Cycle

Effect of Dexmedetomidine on Bispectral Index and Propofol Requirements During Different Menstrual Cycle

Start date: November 2010
Phase: Phase 4
Study type: Interventional

The study was done to evaluate the effects of the follicular and luteal phases of the menstrual cycle on sedation level at loss of consciousness and bispectral index reach to 50 during propofol anesthesia, in patients with and without preoperative intravenous dexmedetomidine .

NCT ID: NCT01927471 Completed - Clinical trials for Polycystic Ovary Syndrome (PCOS)

Nutritional and Metabolic Correlates of Ovarian Morphology in Women With Polycystic Ovary Syndrome

Start date: September 2011
Phase:
Study type: Observational

The investigators would like to determine how aspects of metabolism and age influence ovarian function. The purpose of the study is to understand how nutrition and metabolism relate to follicle development in women with regular cycles, irregular cycles, or polycystic ovary syndrome (PCOS). We also plan to identify lifestyle factors associated with PCOS and understand how diet and activity levels impact features of PCOS.