- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: L thyroxine.
Displaying page 1 of 2.
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: 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: 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: 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: 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: 2014-001369-28 | Sponsor Protocol Number: 880 | Start Date*: 2014-10-30 | |||||||||||
Sponsor Name:Gateshead Health NHS Foundation Trust | |||||||||||||
Full Title: THYRoxine in Acute Myocardial Infarction (ThyrAMI) | |||||||||||||
Medical condition: Hypothyroidism and Acute Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2016-004136-38 | Sponsor Protocol Number: LEVOSOFT_2016 | Start Date*: 2018-07-26 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA SENESE | |||||||||||||
Full Title: PROSPECTIC, RANDOMIZED, NATIONAL MULTICENTRIC STUDY, FINALIZED TO ASSESS THE STABILITY OF TSH LEVELS IN THYROIDECTOMISED PATIENTS IN THERAPY WITH TWO FORMULATIONS OF LEVOTYROXIN (TABLETS AND SOFT-GEL) | |||||||||||||
Medical condition: IATROGENIC HYPOTHYROIDISM IN THYROIDECTOMIZED PATIENTS | |||||||||||||
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Population Age: Adults, Elderly | 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: 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: 2012-004160-22 | Sponsor Protocol Number: LUMC_IEMO80PLUS_1.0 | Start Date*: 2013-06-18 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: IEMO 80-plus thyroid trial | ||
Medical condition: Subclinical hypothyroidism | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004554-26 | Sponsor Protocol Number: GN11GE272 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Multi-modal effects of Thyroid hormone Replacement for Untreated older adults with Subclinical hypothyroidism; a randomised placebo-controlled Trial (TRUST) | |||||||||||||
Medical condition: Subclinical hypothyroidism | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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: 2018-001771-21 | Sponsor Protocol Number: XL184–311 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Exelixis, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Cabozantinib (XL184) in Subjects with Radioiodine-Refractory Differentiated Thyroid Cancer Who Have Progressed after Prior VEGFR-... | |||||||||||||
Medical condition: Radioiodine-Refractory Differentiated Thyroid Cancer which has progressed after prior VEGFR-targeted therapy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) FR (Completed) AT (Prematurely Ended) HU (Completed) ES (Ongoing) PL (Trial now transitioned) CZ (Completed) HR (Completed) GB (GB - no longer in EU/EEA) IT (Completed) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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 |
EudraCT Number: 2021-004594-32 | Sponsor Protocol Number: IO102-IO103-013/MK3475-D18 | Start Date*: 2022-02-16 | |||||||||||
Sponsor Name:IO Biotech ApS | |||||||||||||
Full Title: An open-label, randomized, Phase 3 clinical trial of IO102-IO103 in combination with pembrolizumab versus pembrolizumab alone in patients with previously untreated, unresectable, or metastatic (adv... | |||||||||||||
Medical condition: Patients with previously untreated, unresectable or metastatic (advanced) melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DK (Trial now transitioned) DE (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) IE (Prematurely Ended) BE (Trial now transitioned) HU (Trial now transitioned) PT (Completed) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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