- Trials with a EudraCT protocol (883)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (434)
883 result(s) found for: Endocrine.
Displaying page 1 of 45.
EudraCT Number: 2006-001911-31 | Sponsor Protocol Number: 30032006 | Start Date*: 2007-06-27 | |||||||||||
Sponsor Name:Universitätsfrauenklinik Innsbruck | |||||||||||||
Full Title: Metformin-Wirkung am Ovar bei PCOS (MAO-Studie) - eine Pilotstudie | |||||||||||||
Medical condition: Polycystic ovary syndrome is one of the most common endocrine disorders, affecting approximately 10% of women of reproductive age, associated with hyperandrogenaemia and menstrual dysfunction. The ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022319-20 | Sponsor Protocol Number: 24638418 | Start Date*: 2011-10-13 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: The effect of antidepressant therapy on quality of life, physical and menthal health and cortisole metabolism in PCOS. | |||||||||||||
Medical condition: Polycystic Ovary Syndrome, PCOS, is the most common endocrine disorder in fertile women. Insuliresistance, hirsutism, hyperandrogenemia, adipositas, high cortisole levels and infertility are freque... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004071-39 | Sponsor Protocol Number: TOLV2012 | Start Date*: 2012-10-16 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
Full Title: Study on the effectiveness and safety of the treatment of mild-moderate symptomatic hyponatremia due to syndrome of inappropriate secretion of antidiuretic hormone (SIADH) with Tolvaptan vs fluid ... | |||||||||||||
Medical condition: Mild-moderate symptomatic hyponatremia due to syndrome of inappropriate secretion of antidiuretic hormone (SIADH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004876-20 | Sponsor Protocol Number: GRAV12 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
Full Title: Study on the effectiveness of two different formulations of L-thyroxine compress and liquid oral solution) in pregnant patients affected with hypothyroidism. | |||||||||||||
Medical condition: Hypothyroidism in pregnant patients | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007447-14 | Sponsor Protocol Number: 222500 | Start Date*: 2009-04-03 | ||||||||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI NAPOLI FEDERICO II | ||||||||||||||||||
Full Title: GH-IGF-I status and Multiple Sclerosis: clinical implications (a prevalence study). | ||||||||||||||||||
Medical condition: patients with Multiple Sclerosis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
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: 2020-005605-93 | Sponsor Protocol Number: SILYCUS-21 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:ISTITUTO BIOCHIMICO ITALIANO GIOVANNI LORENZINI S.P.A. | |||||||||||||
Full Title: Efficacy and safety of Silycus® in Cushing’s disease: a multicenter, single arm, open label, dose titration, proof of concept study (Silycus®-21) | |||||||||||||
Medical condition: Cushing's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003027-15 | Sponsor Protocol Number: EFFI2021/01 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:ITALFARMACO S.P.A. | |||||||||||||
Full Title: A multicentre, prospective, open-label, non-comparative study to evaluate menstrual bleeding typology, tolerability, and compliance during a monophasic hormonal contraceptive treatment with norgest... | |||||||||||||
Medical condition: Combined Oral Contraceptives (COC) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000759-91 | Sponsor Protocol Number: PAXO | Start Date*: 2008-04-24 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | ||||||||||||||||||
Full Title: Sorafenib plus paclitaxel metronomic chemotherapy in adreno-cortical-carcinoma patients progressing after 1st or snd line cytotoxic chemotherapy | ||||||||||||||||||
Medical condition: ACC | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008299-14 | Sponsor Protocol Number: IGG-MOMA- 002 | Start Date*: 2009-01-01 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Hypogonadotropic hypogonadism in male newborn | |||||||||||||
Medical condition: MICROPENIS DUE TO HYPOGONADOTROPIC HYPOGONADISM | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019237-10 | Sponsor Protocol Number: FARM8MR2J7 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Multicenter prospective randomized open with a blinded end point (PROBE) parallel-group study on treatment with biphasic insulin BIAsp70/30 and short-acting insulin or rapid-acting analogue plus gl... | |||||||||||||
Medical condition: DM1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020196-23 | Sponsor Protocol Number: EMR 700623-521 | Start Date*: 2011-04-14 | |||||||||||
Sponsor Name:MERCK SERONO SPA | |||||||||||||
Full Title: A phase II, multicentre, open label, prospective, interventional study to evaluate the sperm DNA fragmentation in idiopathic male infertility before and after treatment with Gonal-f PEN 900 IU. | |||||||||||||
Medical condition: Idiophatic male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002240-17 | Sponsor Protocol Number: ATR-101-301 | Start Date*: 2017-05-16 | |||||||||||
Sponsor Name:Millendo Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study of ATR-101 for the Treatment of Cushing’s Syndrome | |||||||||||||
Medical condition: endogenous Cushing’s syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003986-34 | Sponsor Protocol Number: 502.469 | Start Date*: 2005-03-30 | |||||||||||
Sponsor Name:Boehringer Ingelheim Danmark A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group, 16-week MICARDIS® (160 mg) tablets, proof-of-concept study, evaluating insulin sensitivity in overweight or obese, non-diabetic, norm... | |||||||||||||
Medical condition: Overweight or obese, non-diabetic, normotensive subjects | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022821-14 | Sponsor Protocol Number: 2010-022821-14 | Start Date*: 2010-11-11 | ||||||||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||||||||||||||||||
Full Title: Cardiovascular Outcomes of Replacement with Testosterone. Role of testosterone replacement therapy in patients with heart failure. | ||||||||||||||||||
Medical condition: MALE HYPOGONADISM | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005496-39 | Sponsor Protocol Number: APHP211042 | Start Date*: 2021-12-20 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Prospective, randomized, double-blind, placebo controlled, multicenter study assessing the efficacy of intracavernosal Clostridium Botulinum neurotoxin type A (Xeomin®) 100U as add-on therapy to si... | |||||||||||||
Medical condition: Erectile dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001898-78 | Sponsor Protocol Number: CABOTEM | Start Date*: 2020-11-12 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | |||||||||||||
Full Title: A Phase II Single Arm Interventional Trial Evaluating the Activity and Safety of combination between Cabozantinib and Temozolomide in Lung and GEP-NENs progressive after SSAr, everolimus, sunitinib... | |||||||||||||
Medical condition: Patient with Lung and GEP-NENs progressive after SSAr, everolimus, sunitinib or PRRT. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002772-27 | Sponsor Protocol Number: 039(B)PO16143 | Start Date*: 2017-03-20 | |||||||||||||||||||||
Sponsor Name:Angelini S.p.A. | |||||||||||||||||||||||
Full Title: Efficacy and safety of low doses of trazodone in patients affected by painful diabetic neuropathy: randomized, controlled, pilot study. | |||||||||||||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006199-39 | Sponsor Protocol Number: 310523 | Start Date*: 2007-07-05 | |||||||||||
Sponsor Name:Bayer AB, Bayer Schering Pharma | |||||||||||||
Full Title: A double-blind, randomized, multi-center study to investigate the endometrial safety of a continuous, combined, oral estrogen/progestin preparation (0.5 mg 17b-estradiol [E2] / 0.25 mg drospirenone... | |||||||||||||
Medical condition: Women suffering from postmenopausal symptoms | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005055-23 | Sponsor Protocol Number: ENDO-002/08 | Start Date*: 2009-03-05 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO (IRCCS) | |||||||||||||
Full Title: TREATMENT OF HYPERPARATHYROIDISM IN PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 1 (MEN1) WITH THE CALCIMIMETIC AGENT CINACALCET | |||||||||||||
Medical condition: Primary hyperparathyroidism in patients affected with multiple endocrine neoplasia syndrome type 1 (MEN1) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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