- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
15 result(s) found for: L-thyroxine.
Displaying page 1 of 1.
EudraCT Number: 2010-023918-30 | Sponsor Protocol Number: SOMA-001-2010 | Start Date*: 2011-03-16 | |||||||||||
Sponsor Name:SOCIETA' ITALO BRITANNICA L. MANETTI - H.ROBERTS & C. PER AZIONI | |||||||||||||
Full Title: Pilot clinical study on the systemic bioavailability of l-thyroxine in healthy female volunteers after four weeks of topical treatment with a new formulation based on l-thyroxine | |||||||||||||
Medical condition: treatment of localized fat, accompanied by cellulite | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001248-12 | Sponsor Protocol Number: THYR69 | Start Date*: 2015-10-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA MEYER | |||||||||||||
Full Title: Randomized crossover trial for the evaluation of the possible effects in the intestine of two different pharmaceutical forms of L - Thyroxine in patients with primary acquired hypothyroidism | |||||||||||||
Medical condition: Primary acquired hypothyroidism | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023509-37 | Sponsor Protocol Number: IIT2010 | Start Date*: 2011-06-29 |
Sponsor Name:Institut für klinische Forschung und Entwicklung Berlin GmbH am St. Hedwig Krankenhaus | ||
Full Title: A prospective, randomized, single-blind, placebo-controlled, two-armed, phase IV study in patients with subclinical hypothyroidism treated over 52 weeks either with levothyroxine in adjusted dosing... | ||
Medical condition: Subclinical hypothyroidism | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005732-28 | Sponsor Protocol Number: LE-9999-401-BE | Start Date*: 2013-06-14 | ||||||||||||||||
Sponsor Name:Takeda Belgium | ||||||||||||||||||
Full Title: A multicentre, open-label switch study to investigate the necessity of dose adjustment after switching from L-Thyroxine Christiaens® to the new levothyroxine sodium test formulation in (near) total... | ||||||||||||||||||
Medical condition: Patient that underwent a near total thyroidectomy and therefore are compelled to take levothyroxine hormone substition therapy. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002614-36 | Sponsor Protocol Number: 05ICHF/T407 | Start Date*: 2007-04-20 | |||||||||||
Sponsor Name:IBSA | |||||||||||||
Full Title: Multicentre, controlled, randomised, open-label, cross-over clinical study of the efficacy and tolerability of L-thyroxine T4 soft capsules, in comparison to L-thyroxine tablets, in thyroidectomi... | |||||||||||||
Medical condition: Substitutive and/or TSH suppressive therapy in thyroidectomized patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021228-89 | Sponsor Protocol Number: CICO-10-01 | Start Date*: 2011-04-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Effect of L-Thyroxine supplementation in the first weeks of life on long-term neurodevelopmental outcome in infants with transient hypothyroxinemia born at or less than 28 weeks’ gestation | |||||||||||||
Medical condition: infants with transient hypothyroxinemia born at or less than 28 weeks’ gestation | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001696-21 | Sponsor Protocol Number: AOBS-2MED-TICO-2013 | Start Date*: 2013-08-20 |
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | ||
Full Title: Prospective blinded study of the absorption of levothyroxine oral solution (Tirosint ® single-dose oral solution) in patients with hypothyroidism. | ||
Medical condition: Hypothyrodism | ||
Disease: | ||
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: 2009-018277-31 | Sponsor Protocol Number: AOI/2009/VT-03 | Start Date*: 2010-02-18 |
Sponsor Name:CHU de Nîmes | ||
Full Title: EVALUATION DU RETENTISSEMENT PSYCHIATRIQUE, CARDIOVASCULAIRE ET SUR LA QUALITE DE VIE DE L’ HORMONOTHERAPIE FREINATRICE DANS UNE COHORTE DE PATIENTS THYROIDECTOMISES POUR CARCINOME THYROIDIEN PAPI... | ||
Medical condition: Thyroidectomie pour carcinome papillaire différencié | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018663-42 | Sponsor Protocol Number: T3S01-10 | Start Date*: 2010-06-15 | |||||||||||
Sponsor Name:BRACCO | |||||||||||||
Full Title: Substitutive therapy of hypothyroid patients with L-thyroxine (T4) plus T3 sulfate (T3S). A Phase II, open-label, single centre, parallel group study on therapeutic efficacy and tolerability | |||||||||||||
Medical condition: Thyroidectomized patients without endogenous hormonal production (Tg<5) in stable substitutive therapy with T4 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002127-26 | Sponsor Protocol Number: BAFFI_14 | Start Date*: 2015-10-13 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | |||||||||||||
Full Title: Randomized, single-blind, controlled study of the anti-BAFF antibody belimumab or methylprednisolone treatment in hyperthyroid Graves' disease (GD) and active orbitopathy (GO) | |||||||||||||
Medical condition: GRAVES' ORBITOPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004334-99 | Sponsor Protocol Number: 151201 | Start Date*: 2016-02-01 |
Sponsor Name:Department of Endocrinology | ||
Full Title: Treatment of Graves´ ophthalmopathy with diclofenak or simvastatin | ||
Medical condition: Graves´ophthalmopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002790-22 | Sponsor Protocol Number: ML39921 | Start Date*: 2019-04-11 | ||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | ||||||||||||||||||
Full Title: Tocilizumab in Graves’ Orbitopathy (TOGO). Multicenter, randomized, observer-blind, controlled study of the anti-IL-6 receptor antibody tocilizumab (TCZ) or methylprednisolone (MP) treatment in pat... | ||||||||||||||||||
Medical condition: Active moderate-severe Graves' Orbitopathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001107-38 | Sponsor Protocol Number: SESCHI.26371 | Start Date*: 2008-05-26 | |||||||||||
Sponsor Name:Cefak KG | |||||||||||||
Full Title: Dose finding study to investigate efficacy and tolerability of a 6 month oral treatment with selenium in patients with autoimmune thyroiditis: prospective, controlled parallel group study with Cef... | |||||||||||||
Medical condition: Autoimmune thyroiditis (Hashimoto-thyroiditis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004425-27 | Sponsor Protocol Number: 5863 | Start Date*: 2012-05-29 |
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: Study of Optimal Replacement of Thyroxine in the ElDerly (SORTED) SORTED 1 – a Randomised Controlled Trial (Pilot study) SORTED 2 – Qualitative Interviews SORTED 3 – Retrospective Cohort | ||
Medical condition: hypothyroidism (elderly individuals) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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