- Trials with a EudraCT protocol (35)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (63)
35 result(s) found for: Cortisone.
Displaying page 1 of 2.
EudraCT Number: 2021-006487-24 | Sponsor Protocol Number: ADNorGC | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Helse Bergen HF | |||||||||||||
Full Title: A registry-based, open-label, randomized study to investigate quality-of-life with Plenadren compared with Cortison in participants aged 16-80 with newly diagnosed primary adrenal insufficiency | |||||||||||||
Medical condition: Primary adrenal insufficiency | |||||||||||||
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Population Age: Adolescents, Under 18, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000866-40 | Sponsor Protocol Number: 2012-000866-40 | Start Date*: 2012-03-12 | |||||||||||
Sponsor Name:ISTITUTO ORTOPEDICO RIZZOLI | |||||||||||||
Full Title: Evaluation of the efficacy and suppression of the hypothalamic-pituitary-adrenal axis resulting in intrabursale single administration of cortisone in patients with calcific tendonitis of the rotato... | |||||||||||||
Medical condition: calcific tendonitis of the rotator cuff | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004187-35 | Sponsor Protocol Number: FACE-01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Falun Hospital | |||||||||||||
Full Title: The FACE (Facial nerve palsy And Cortisone Evaluation) study in children: a randomised double-blind, placebo-controlled, multicenter trial. | |||||||||||||
Medical condition: Facial Nerve Palsy (Bells Palsy) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004232-37 | Sponsor Protocol Number: Metylpred-01 | Start Date*: 2012-11-29 |
Sponsor Name:Sahlgrenska Universtitetssjukhuset/SUS | ||
Full Title: Prophylactic treatment with methylprednisolone may reduce the cerebral inflammatory response and reduce the severity of cognitive dysfunction after cardiac surgery | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001900-76 | Sponsor Protocol Number: PRASCO | Start Date*: 2015-08-25 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Manipulating the microbiome in IBD by antibiotics and fecal microbiota transplantation (FMT): a randomized controlled trial | |||||||||||||
Medical condition: Acute Severe colitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000344-25 | Sponsor Protocol Number: 17-249 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Essai, randomisé, contrôlé, ouvert, de deux schémas standardisés de décroissance, respectivement rapide (nord-américain) et lent (européen), de cortisone dans l’artérite à cellules géantes. | |||||||||||||
Medical condition: Patients atteints d’artérite à cellules géantes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005484-32 | Sponsor Protocol Number: VN-FT-01 | Start Date*: 2015-05-28 | ||||||||||||||||||||||||||
Sponsor Name:Lund University | ||||||||||||||||||||||||||||
Full Title: Double-blind, randomized placebo controlled study on the effect from cortisone treatment of vestibular neuritis - function, subjective well-being and stress | ||||||||||||||||||||||||||||
Medical condition: Acute vestibular syndrome better known as Vestibular neuritis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004515-12 | Sponsor Protocol Number: 00174 | Start Date*: 2017-03-31 |
Sponsor Name:Raimo Tuuminen | ||
Full Title: Comparison between peri- and post-operative anti-inflammatory medication in cataract surgery: a randomized clinical trial | ||
Medical condition: Cataract senilis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002658-19 | Sponsor Protocol Number: 20016-01 | Start Date*: 2018-06-25 |
Sponsor Name:Department für Kinder- und Jugendheilkunde, Pädiatrie I | ||
Full Title: Influence of pulsatile dexamethasone therapy in childhood epilepsia on the immune Systeme. | ||
Medical condition: Analization of specific immune cells and immune modulation factors in children under pulsatile dexamethasone-therapy. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006515-23 | Sponsor Protocol Number: STC- Progesterone -2007 | Start Date*: 2008-01-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: Randomized clinical trial for the local therapy of carpal tunnel syndrome: cortisone vs progesterone | |||||||||||||
Medical condition: - mild-to-moderate idiopathic carpal tunnel syndrome | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001749-13 | Sponsor Protocol Number: P04071 | Start Date*: 2005-02-22 |
Sponsor Name:AESCA Pharma GesmbH | ||
Full Title: Randomized Phase II Study: Temozolomide (TMZ) Concomitant to Radiotherapy followed by sequential TMZ in Advanced NSCLC Patients with CNS Metastasis versus Radiotherapy alone | ||
Medical condition: Patients with non small cell lung cancer (NSCLC) have a high risk of developing brain metastasis, up to 40% as evaluated in autopsy studies. These patients are often heavily symptomatic and their l... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-002585-32 | Sponsor Protocol Number: Mpp01 | Start Date*: 2017-11-15 |
Sponsor Name:Infektionskliniken Danderyds sjukhus AB | ||
Full Title: A randomised, multicentre, controlled trial to study the duration of supplemental oxygen treatment in adults with Mycoplasma pneumoniae pneumonia treated with betamethasone in addition to antibiotics | ||
Medical condition: Mycoplasma pneumoniae pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001186-42 | Sponsor Protocol Number: 260114BS, ASF 1075-203 | Start Date*: 2006-07-21 |
Sponsor Name:Astion Danmark A/S | ||
Full Title: Determination of antipsoriatic efficacy of topical formulations in a psoriasis plaque test | ||
Medical condition: male or female subjects with chronic plaque type psoriasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022640-20 | Sponsor Protocol Number: JL23 | Start Date*: 2011-01-12 | |||||||||||
Sponsor Name:Johanna Laukkarinen | |||||||||||||
Full Title: Cortisone treatment for the prevention of postoperative pancreatitis and pancreatitis-induced complications after pancreaticoduodenectomy (Whipple operation). | |||||||||||||
Medical condition: Tutkittavat potilaat ovat leikkauspotilaita, joille suoritetaan rutiinisti haimanpään-ja pohjukaissuolen poistoleikkaus (Whipplen operaatio) joko kasvaimen tai kroonisen haimatulehduksen vuoksi. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018639-17 | Sponsor Protocol Number: UR2010MSyn | Start Date*: 2010-06-29 | |||||||||||
Sponsor Name:University Hospital Erlangen | |||||||||||||
Full Title: Prospective and open label study with blind end point evaluation on the effect of mineralcorticoid receptor inhibition on endothelial function of the micro- and macrovasculature in patient with met... | |||||||||||||
Medical condition: Metabolic syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001217-25 | Sponsor Protocol Number: 2016-001217-25 | Start Date*: 2016-09-07 |
Sponsor Name:Uppsala University | ||
Full Title: Emotion, Serotonin and Premenstrual Dysphoric Disorder (EmSeP) | ||
Medical condition: Premenstrual Dysphoric Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004028-12 | Sponsor Protocol Number: PLEN2013 | Start Date*: 2014-05-13 | |||||||||||
Sponsor Name:Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico | |||||||||||||
Full Title: Replacement therapy with modified-release hydrocortisone (Plenadren) in patients with central adrenal insufficiency | |||||||||||||
Medical condition: Central hypoadrenalism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002202-18 | Sponsor Protocol Number: INT 07/07 | Start Date*: 2008-01-11 | ||||||||||||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||||||||||||
Full Title: CALENDULA POMADE VERSUS PLACEBO CREAM/CORTISONE CREAM (FLUORCORTOLONE) IN THE PREVENTION OF CUTANEOUS ERYTHEMA DUE TO BREAST IRRADIATION. A RANDOMIZED STUDY ON 60 PATIENTS | ||||||||||||||||||||||||||||
Medical condition: Patients treated for the first time with radiotherapy to the residual breast after quadrantectomy for proven non-metastatic breast cancer. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006184-19 | Sponsor Protocol Number: SPI-62-CL-2001 | Start Date*: 2022-06-22 | |||||||||||
Sponsor Name:Sparrow Pharmaceuticals, Inc. | |||||||||||||
Full Title: SPI-62 as a Treatment for Adrenocorticotropic Hormone-dependent Cushing’s Syndrome | |||||||||||||
Medical condition: Cushing’s Syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000144-21 | Sponsor Protocol Number: DIUR-016-AI | Start Date*: 2022-01-14 | |||||||||||
Sponsor Name:Diurnal Limited | |||||||||||||
Full Title: A Double-Blind, Double-Dummy, Two-Way Cross-Over, Randomised, Phase II Study of Efficacy, Safety and Tolerability of Modified-Release Hydrocortisones: Chronocort® Versus Plenadren®, in Adrenal Insu... | |||||||||||||
Medical condition: Adrenal Insufficiency (AI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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