| Status | Study |
| Not yet recruiting |
Study Name: Compare the Different Routes of Administration of Misoprostol During Medicinal Abortion Between 7 and 9 Weeks of Amenorrhoea (SA) Condition: Misoprostol Drug-induced Abortion Date: 2017-04-27 Interventions: Biological: Assess the efficacy and side effects of Misoprostol according to the route of administration |
| Recruiting |
Study Name: The Health of Competitive Fitness Athletes Condition: Resting Metabolic Rate Bone Mineral Density, Low, Susceptibility to Date: 2016-12-24 Interventions: Other: Psychological health Ob |
| Recruiting |
Study Name: Atherosclerosis, Immune Mediated Inflammation and Hypoestrogenemia in Young Women Condition: Estrogen Deficiency Cardiovascular Disease (CVD) Hypothala Date: 2016-12-01 Interventions: Drug: 17beta Estradiol Partici |
| Recruiting |
Study Name: CaREFREE Study (Calorie Restriction, Environment and Fitness: Reproductive Effects Evaluation Study) Condition: Normal Physiology Healthy Date: 2016-08-05 Interventions: Behavioral: NEA Neutral Energy |
| Not yet recruiting |
Study Name: Pubertal Induction in Individuals With Hypogonadism Condition: Primary Amenorrhoea Hypothalamic Amenorrh Date: 2016-07-26 Interventions: Drug: Routine transdermal oestrogen patch Transdermal oestrogen patch will be used with an incremental d |
| Recruiting |
Study Name: Estradiol and Fear Extinction in Anorexia Nervosa (AN) Condition: Anorexia Nervosa Date: 2016-05-23 Interventions: Drug: Estradiol AN participants will be prescribed 28 days of transdermal estradiol 0.1 mg/d (Days 1-28) |
| Recruiting |
Study Name: Total Antioxidant Capacity Before and After HRT in Hypotalamic Amenorrhea Condition: Hypothalamic Amenorrhea Date: 2016-03-05 Interventions: Drug: 1 mg of transdermal estradiol daily and 10mg of oral MPA |
| Recruiting |
Study Name: Rejuvenation of Premature Ovarian Failure With Stem Cells Condition: Premature Ovarian Failure Date: 2016-02-16 Interventions: Procedure: ROSE Protocol Laparoscopy followed by injection of BMSC fraction in right ovary |
| Recruiting |
Study Name: Impact of Oropharyngeal Administration of Colostrum in the First 48 Hours of Life Term Premature Newborn ≤ 32 Weeks of Amenorrhea Condition: Infant, Premature Date: 2016-01-06 Interventions: Biological: Colostrum feeding Biological: |
| Completed |
Study Name: Efficacy of Mifepristone - Prostaglandin Analogue Combination in Medical Termination of Pregnancy Beyond 7 Weeks of Amenorrhea Condition: Medical Termination of Pregnancy Date: 2015-11-20 |