- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
17 result(s) found for: Hydrocortisone Acetate.
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EudraCT Number: 2010-019178-33 | Sponsor Protocol Number: BRD/10/1-L | Start Date*: 2010-05-27 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: Traitement de l'insuffisance surrénale secondaire à un traumatisme crânien grave. Etude multicentrique, contrôlée, randomisée portant sur un médicament. - Etude Corti-TC" | |||||||||||||
Medical condition: Insuffisance surrénale secondaire à un traumatisme crânien grave | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002471-32 | Sponsor Protocol Number: S173-GB-01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Stiefel Laboratories Maidenhead Ltd (commonly known as Stiefel International R&D) | |||||||||||||
Full Title: A PHASE II, SINGLE-CENTRE, INVESTIGATOR-BLIND, PARALLEL GROUP CLINICAL TRIAL TO INVESTIGATE THE EFFICACY AND SAFETY OF 1% CICLOPIROX OLAMINE (BATRAFEN® CREAM), COMPARED TO 1% HYDROCORTISONE ACETATE... | |||||||||||||
Medical condition: Mild to moderate atopic eczema | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
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: 2004-003734-34 | Sponsor Protocol Number: BT0800BEL001 | Start Date*: 2005-03-03 |
Sponsor Name:Barrier Therapeutics nv | ||
Full Title: A one-weel, randomized, double-blind, placebo-controlled pilot trial to evaluate oral R129160 (60 mg b.i.d.) on the alleviation of itch in atopic dermatitis patients | ||
Medical condition: Atopic Dermatitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Ongoing) CZ (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003596-19 | Sponsor Protocol Number: CHS1221 | Start Date*: 2020-07-29 | |||||||||||||||||||||||||||||||
Sponsor Name:Cristcot HCA LLC | |||||||||||||||||||||||||||||||||
Full Title: A Three-Arm, Randomized, Placebo-Controlled, Double-Blind Phase 3 Study to Evaluate the Safety and Efficacy of Once-Daily and Twice-Daily Dosing of a Novel Hydrocortisone Acetate 90 mg Suppository ... | |||||||||||||||||||||||||||||||||
Medical condition: Ulcerative Colitis of the Rectum | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) RO (Ongoing) DK (Ongoing) BG (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001175-38 | Sponsor Protocol Number: 6520-9170-08 | Start Date*: 2012-01-13 |
Sponsor Name:MEDICE Arzneimittel Pütter GmbH & CO.KG | ||
Full Title: A multi-center, randomized, double-blind,phase II trial with intraindividual comparison to assess superiority of Soventol HydroCort 0.5 % Cremogel vs vehicle on lesional skin in patients with mild ... | ||
Medical condition: manifest atopic dermatitis diagnosed according to Hanifin and Rajka, or seborrheic eczema or stasis dermatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004485-40 | Sponsor Protocol Number: P070128 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Etude prospective, multicentrique contrôlée vs placebo, randomisée, en double insu comparant la protéine C activée, les faibles doses de corticoïdes et leur association dans le traitement du choc s... | |||||||||||||
Medical condition: Choc septique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004759-39 | Sponsor Protocol Number: 06-02/Nyco-P | Start Date*: 2007-11-26 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Doppelblinde, randomisierte klinische Studie zum Vergleich der Wirksamkeit und Verträglichkeit einer Nystatin (100 000 I.E./g)/Hydrocortisonacetat (5 mg/g) -haltigen Paste vs. einer Nystatin (100 0... | |||||||||||||
Medical condition: Adult patients with moderate to severe inflamed candidiasis of the skin | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004542-28 | Sponsor Protocol Number: NL59862.091.16 | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: A randomized controlled pilot study comparing the efficacy of topical coal tar to topical corticosteroids in children aged 1 to < 16 years with moderate-severe atopic dermatitis. | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003900-28 | Sponsor Protocol Number: TOFA-PREDICT | Start Date*: 2018-04-04 |
Sponsor Name:UMC Utrecht | ||
Full Title: A Stratification trial to determine key immunological factors predicting Tofacitinib efficacy in Psoriatic Arthritis (PsA). TOFA-PREDICT | ||
Medical condition: psoriatic arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003024-20 | Sponsor Protocol Number: HEMP-0119/ES | Start Date*: 2019-10-15 |
Sponsor Name:FAES FARMA SA | ||
Full Title: Multicenter, double-blind, randomized clinical trial to evaluate and compare the efficacy and safety of Hemorrane® Plus (Hemorrane® + benzocaine) with Hemorrane® and with placebo in patients with g... | ||
Medical condition: Bleeding grade I hemorrhoids | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005066-32 | Sponsor Protocol Number: 80-82310-98-09036 | Start Date*: 2009-02-03 | |||||||||||
Sponsor Name:University Medical Center | |||||||||||||
Full Title: Comparison of ototopical antibiotic-steroid drops or oral antibiotics versus watchful waiting in children with acute tympanostomy tube otorrhea | |||||||||||||
Medical condition: Acute tympanostomy tube otorrhea in children | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004765-40 | Sponsor Protocol Number: SPR001-204 | Start Date*: 2020-11-17 | |||||||||||
Sponsor Name:Spruce Biosciences, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SPR001 (Tildacerfont) in Reducing Supraphysiologic Glucocorticoid Use in Adult Subjects with Classic Co... | |||||||||||||
Medical condition: Classic Congenital Adrenal Hyperplasia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) NL (Trial now transitioned) DE (Ongoing) SE (Trial now transitioned) PL (Trial now transitioned) LT (Trial now transitioned) IT (Ongoing) EE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001438-46 | Sponsor Protocol Number: A3921104 | Start Date*: 2018-03-27 | |||||||||||
Sponsor Name:Pfizer Inc. | |||||||||||||
Full Title: EFFICACY, SAFETY AND TOLERABILITY OF TOFACITINIB FOR TREATMENT OF POLYARTICULAR COURSE JUVENILE IDIOPATHIC ARTHRITIS (JIA) IN CHILDREN AND ADOLESCENT SUBJECTS | |||||||||||||
Medical condition: JUVENILE IDIOPATHIC ARTHRITIS (JIA) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000839-17 | Sponsor Protocol Number: CASM981C2439 | Start Date*: 2005-04-11 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 16-week, randomized, multi-center, parallel-group, pimecrolimus-blinded, controlled study (4-week treatment period followed by 12-week observational period) to evaluate the safety of concomitant ... | |||||||||||||
Medical condition: Treatment of severe atopic dermatitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004764-22 | Sponsor Protocol Number: SPR001-203 | Start Date*: 2020-10-15 | |||||||||||
Sponsor Name:Spruce Biosciences, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy and Safety of SPR001 (Tildacerfont) in Adult Subjects with Classic Congenital Adrenal Hyperplasia | |||||||||||||
Medical condition: Classic Congenital Adrenal Hyperplasia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) SE (Trial now transitioned) DE (Ongoing) DK (Trial now transitioned) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) IT (Ongoing) LT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000984-34 | Sponsor Protocol Number: 6630-9170-917016 | Start Date*: 2018-05-24 | |||||||||||||||||||||
Sponsor Name:Medice Arzneimittel Pütter GmbH & Co KG | |||||||||||||||||||||||
Full Title: A multi-center, randomized, double-blind, phase II trial with intraindividual comparison to assess superiority of Soventol HydroCortisonACETAT 1 % Cremogel versus vehicle on lesional skin in patien... | |||||||||||||||||||||||
Medical condition: atopic dermatitis, seborrheic eczema or stasis dermatitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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