- Trials with a EudraCT protocol (124)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
124 result(s) found for: Steroid Hormone.
Displaying page 1 of 7.
| EudraCT Number: 2015-005762-28 | Sponsor Protocol Number: 1512-VLC-066-EB | Start Date*: 2016-04-06 |
| Sponsor Name:IVI Valencia | ||
| Full Title: Analysis of follicular steroid synthesis during controlled ovarian stimulation with recombinant FSH vs HMG in GnRH antagonist cycles | ||
| Medical condition: Women undergoing ovarian stimulation for oocyte donation | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001988-23 | Sponsor Protocol Number: AEZS-130-P01 | Start Date*: 2018-11-07 | |||||||||||
| Sponsor Name:Aeterna Zentaris GmbH | |||||||||||||
| Full Title: Open label, group comparison, dose escalation trial to investigate safety, tolerability, pharmacokinetics and pharmacodynamics of macimorelin acetate after single oral dosing of 0.25 mg/kg, 0.5 mg/... | |||||||||||||
| Medical condition: Diagnosis of Growth Hormone Deficiency | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003254-76 | Sponsor Protocol Number: 20200518 | Start Date*: 2020-09-09 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: Effects of local dehydroepiandrosterone (DHEA) and estradiol on moderate to severe dyspareunia, a symptom of vulvovaginal atrophy in postmenopausal women - a randomized, controlled study | ||
| Medical condition: Vulvovaginal atrophy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001370-20 | Sponsor Protocol Number: OPV116910 | Start Date*: 2014-11-26 | |||||||||||
| Sponsor Name:Glaxo Group Ltd | |||||||||||||
| Full Title: OPV116910: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Investigate the Efficacy and Safety of Ofatumumab Injection for Subcutaneous Use in Subjects with Pemphigus Vulgaris | |||||||||||||
| Medical condition: Pemphigus Vulgaris | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) HR (Completed) GR (Completed) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005685-12 | Sponsor Protocol Number: 20070724 | Start Date*: 2008-10-09 |
| Sponsor Name:Universitätsklinik für Psychiatrie und Psychotherapie, Klin. Abteilung f. Biologische Psychiatrie | ||
| Full Title: The influence of hormone replacement therapy on the cerebral serotonin-1A receptor distribution and mood in postmenopausal women | ||
| Medical condition: Healthy postmenopausal women receiving standard hormone replacement therapy are measured using positron emission tomography to investigate the effects of hormones on the cerebral serotonin-1A recep... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-004889-10 | Sponsor Protocol Number: DapaFIT | Start Date*: 2021-04-28 |
| Sponsor Name:University Hospital Tuebingen | ||
| Full Title: Dapagliflozin effect on erythropoiesis and physical fitness in patients with type 2 diabetes - a randomized, partly double-blinded, controlled, three armed, parallel group, exploratory study | ||
| Medical condition: Patients with T2DM and hypertension aged 40 to 70 years (including) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012218-30 | Sponsor Protocol Number: ML22648 | Start Date*: 2009-10-06 |
| Sponsor Name:Roche Farmacêutica Química, Lda. | ||
| Full Title: A randomized, double-blind, placebo-controlled study to assess the efficacy of tocilizumab (TCZ) + non-biological DMARD in reducing synovitis as measured by magnetic resonance imaging (MRI) at 12 w... | ||
| Medical condition: Men and women > 18 years of age with RA who are currently experiencing an inadequate clinical response to a stable dose of non-biologic DMARDs (at least 12 weeks) and with MRI documented synovitis ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-002785-20 | Sponsor Protocol Number: EVIDIMS | Start Date*: 2011-09-19 |
| Sponsor Name:Charité - Universitätsmedizin Berlin | ||
| Full Title: Efficacy of Vitamin D Supplementation in relapsing-remitting Multiple Sclerosis | ||
| Medical condition: Multiple Sclerosis and Clinical isolated Syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004553-60 | Sponsor Protocol Number: CP-4-004 | Start Date*: 2012-01-10 |
| Sponsor Name:OPKO Biologics Ltd. | ||
| Full Title: Safety and dose finding study of different MOD-4023 dose levels compared to daily r-hGH therapy in pre-pubertal growth hormone deficient children | ||
| Medical condition: Pediatric Growth Hormone Deficiency | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: HU (Completed) SK (Ongoing) CZ (Prematurely Ended) GR (Completed) PL (Completed) BG (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005240-10 | Sponsor Protocol Number: C/24/2011 | Start Date*: 2012-03-27 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: A phase II, open label, preoperative study to assess the efficacy of the novel steroid sulfatase inhibitor Irosustat in postmenopausal women with early oestrogen receptor positive breast cancer. | |||||||||||||
| Medical condition: Breast Cancer, ER positive, early | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001016-51 | Sponsor Protocol Number: 05-UTROGEL-01 | Start Date*: 2006-02-28 |
| Sponsor Name:Karolinska Hospital | ||
| Full Title: In vivo effects of transdermal Estradiol+ oral Progesterone vs oral Conjugated Equine Estrogens + MedroxyProgesteroneAcetate on normal human breast cells proliferation: a randomized comparative study | ||
| Medical condition: Menopausal symptoms | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-004189-33 | Sponsor Protocol Number: REK322442 | Start Date*: 2013-11-28 |
| Sponsor Name:Haukeland University Hospital | ||
| Full Title: ULTRADIAN SUBCUTANEOUS HYDROCORTISONE (USHI) INFUSION IN ADDISON’S DISEASE | ||
| Medical condition: Addison`s disease | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000790-24 | Sponsor Protocol Number: BEC01 | Start Date*: 2020-07-14 | |||||||||||||||||||||
| Sponsor Name:Universität Salzburg | |||||||||||||||||||||||
| Full Title: BECONTRA - Effects of combined oral contraceptives on brain and behavior | |||||||||||||||||||||||
| Medical condition: Girls and women 14 years - 35 years, considering the intake of COCs or under current use of EE/LNG or EE/CMA COCs | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||||||||||||
| Trial protocol: AT (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2009-010632-18 | Sponsor Protocol Number: 022009endo | Start Date*: 2009-05-21 | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
| Full Title: EFFECT OF ORAL OR INTRAVENOUS STEROID PROPHYLAXIS ON THE OCCURRENCE OF GRAVES ORBITOPATHY IN PATIENTS WITH GRAVES DISEASE AFTER TREATMENT WITH RADIOACTIVE IODINE | |||||||||||||
| Medical condition: Graves orbitopathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010288-17 | Sponsor Protocol Number: 1516 | Start Date*: 2009-07-13 |
| Sponsor Name:Karolinska Hospital | ||
| Full Title: Breast cell turnover and mammographic density in women with Polycystic Ovary Syndrome (PCOS) | ||
| Medical condition: Polycystic ovary syndrome (PCOS) is the most common hormonal aberration in women of fertile age, with a prevalence of 5-10%, and is associated with chronic anovulation, hyperandrogenism and PCO mo... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-015538-30 | Sponsor Protocol Number: OXTsozphob | Start Date*: 2010-04-21 | |||||||||||
| Sponsor Name:Rheinisch-Westfälisch Technische Hochschule Aachen | |||||||||||||
| Full Title: Effect of intranasal oxytocin on social approach in patients with social phobia and healthy control | |||||||||||||
| Medical condition: The effect of oxytocin is investigated in social processing of social phobic patient and healthy controls | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004874-42 | Sponsor Protocol Number: TRAFO001 | Start Date*: 2009-02-06 | |||||||||||
| Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||
| Full Title: Evaluation of predictive Factors for the Effectivity of Aromatase Inhibitor Therapy - Offene, prospektive, multizentrische Phase IV-Studie zur Untersuchung des Einflusses von pharmakogenetischen M... | |||||||||||||
| Medical condition: The study examines the influence of pharmacogenetic markers on the efficacy and side effects in postmenopausal, steroid hormone positive breast cancer patients, who are treated with Letrozol. The p... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003060-40 | Sponsor Protocol Number: TICSI | Start Date*: 2017-01-17 | |||||||||||
| Sponsor Name:University of Oxford, Clinical Trials and Research Governance | |||||||||||||
| Full Title: Targeting Iatrogenic Cushing’s Syndrome with 11β-hydroxysteroid dehydrogenase type 1 Inhibition | |||||||||||||
| Medical condition: Adverse effects of prescribed glucocorticoid therapy | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000178-20 | Sponsor Protocol Number: MCT8-2014-1 | Start Date*: 2015-08-12 |
| Sponsor Name:Erasmus Medical Centre | ||
| Full Title: Thyroid hormone analog therapy of patients with severe psychomotor retardation caused by mutations in the MCT8 thyroid hormone transporter: The Triac Trial. | ||
| Medical condition: This therapuetical trial will be conducted in patient with the Allan-Herndon-Dudley Syndrome (AHDS), casued by mutations in the thyroid hormone transporter MCT8. This results in the characteristic ... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male | |
| Trial protocol: BE (Completed) CZ (Completed) DE (Completed) IT (Completed) FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006082-32 | Sponsor Protocol Number: 2293/2007 | Start Date*: 2007-12-13 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
| Full Title: Female steroid hormones and protection from cardiovascular risk: staminal endothelial progenitor cells and menopause. | |||||||||||||
| Medical condition: Postmenopause | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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