- Trials with a EudraCT protocol (847)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (124)
847 result(s) found for: Dexamethasone.
Displaying page 6 of 43.
EudraCT Number: 2004-002502-29 | Sponsor Protocol Number: 206207-009 | Start Date*: 2004-12-08 |
Sponsor Name:Allergan Limited | ||
Full Title: A Six-Month Phase 3, Multicenter, Masked, Randomized, Sham-Controlled Trial (with Six-Month Open-Label Extension) to Assess the Safety and Efficacy of 700 µg and 350 µg Dexamethasone Posterior Segm... | ||
Medical condition: Macular edema due to Branch Retinal Vein Occlusion (BRVO) or Central Retinal Vein Occlusion (CRVO) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002185-51 | Sponsor Protocol Number: Poplitea2017 | Start Date*: 2017-10-18 | |||||||||||
Sponsor Name:Tampere University Hospital | |||||||||||||
Full Title: Effect of perineural dexamethasone on the duration of popliteal nerve block for analgesia after ankle surgery | |||||||||||||
Medical condition: Ankle arthrosis, situation after ankle injury or malposition of ankle/foot, arthrodesis as a curative therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000388-10 | Sponsor Protocol Number: RF-2010-2318192 | Start Date*: 2013-03-30 |
Sponsor Name:AZIENDA ULSS N.9 - TREVISO, UOC PEDIATRIA | ||
Full Title: Oral steroids for reducing renal scarring in infants with febrile urinary tract infections at high risk for renal scar development: a randomized controlled trial | ||
Medical condition: Infants with febrile UTI at higher risk for renal scar development based on PCT values ≥ 1 ng/mL | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005789-38 | Sponsor Protocol Number: HU03/ANE/DEXA | Start Date*: 2006-12-11 | |||||||||||
Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola (H.U.D.E.R.F.) | |||||||||||||
Full Title: Dexaméthasone et Amygdalectomie | |||||||||||||
Medical condition: Children aged from 2 to 8 years old requiring tonsillectomy | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002815-32 | Sponsor Protocol Number: DXMPN2017 | Start Date*: 2017-10-05 |
Sponsor Name:AZ Groeninge | ||
Full Title: The dose response of Dexamethasone as perineural adjuvant in Brachial Plexus Block. | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000202-29 | Sponsor Protocol Number: 2CA_2019_ORL_01 | Start Date*: 2020-07-27 | |||||||||||
Sponsor Name: Centro Clínico Académico - Braga, Associação (2CA-Braga) | |||||||||||||
Full Title: Single-center, double-blind, placebo-controlled study evaluating the efficacy of pre-incisional local analgesia with ropivacaine and dexamethasone for pain management after tonsillectomy | |||||||||||||
Medical condition: Patients selected for tonsillectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004763-31 | Sponsor Protocol Number: CRO.CO.DEX | Start Date*: Information not available in EudraCT |
Sponsor Name:EryDel S.p.A. | ||
Full Title: Therapy with dexamethasone intra-erythrocytes in patients with Crohn disease and ulcerative colitis | ||
Medical condition: patients with Crohn’s Disease and Ulcerative Colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000395-41 | Sponsor Protocol Number: ICORG 05-01 | Start Date*: 2005-05-27 |
Sponsor Name:All Ireland co-operative Oncology Research Group | ||
Full Title: Phase II Study to Assess the Safety, Efficacy, and Tolerability of Combination Therapy with Velcade (Bortezomib), Adriamycin, and Dexamethasone (PAD) as Therapy for Patients with relapsed or refra... | ||
Medical condition: Relapsed or refractory Multiple Myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003595-23 | Sponsor Protocol Number: CIP-DEX/001/14 | Start Date*: 2014-12-17 | |||||||||||
Sponsor Name:Watson Laboratories Inc. | |||||||||||||
Full Title: A double-blinded, parallel-group, randomized, single dose study to assess the pharmacokinetic bioequivalence of ciprofloxacin (0.3%) and dexamethasone (0.1%) otic suspension (Indoco for Actavis) ve... | |||||||||||||
Medical condition: Patients with current or previous history of acute otitis media (AOM) and recurrent acute otitis media (RAOM). | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006421-13 | Sponsor Protocol Number: BBD | Start Date*: 2008-11-28 |
Sponsor Name:Wilhelminen Krebsforschung GmbH | ||
Full Title: Multicenter Phase II Study: Bendamustine plus Bortezomib plus Dexamethasone in the treatment of stage II/III relapsed or refractory multiple myeloma | ||
Medical condition: Patients suffering from stage II/III (Salmon & Durie) relapsed or refractory multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001702-18 | Sponsor Protocol Number: protocol1tdn | Start Date*: 2014-08-28 | |||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | |||||||||||||
Full Title: Analgesic duration of a preoperative single-shot femoral nerve block with Bupivacaine and adjuvant Dexamethasone in patients with hip fracture | |||||||||||||
Medical condition: Pain in patients with hip fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002190-25 | Sponsor Protocol Number: GEM-IBERDARAX | Start Date*: 2022-06-09 |
Sponsor Name:Fundacion PETHEMA | ||
Full Title: Multicenter, phase II, national and open-label study to evaluate Iberdomide-dexamethasone alone or in combination with standard MM treatment regimens in transplant ineligible newly diagnosed patients | ||
Medical condition: Multiple Myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001940-37 | Sponsor Protocol Number: EFC15246 | Start Date*: 2017-12-13 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: Randomized, Open Label, Multicenter Study Assessing The Clinical Benefit Of Isatuximab Combined With Carfilzomib (Kyprolis®) And Dexamethasone Versus Carfilzomib With Dexamethasone In Patients Wit... | |||||||||||||
Medical condition: Plasma cell myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) HU (Completed) ES (Ongoing) FR (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000736-26 | Sponsor Protocol Number: 206207-014 | Start Date*: 2006-05-17 |
Sponsor Name:Allergan Limited | ||
Full Title: An 8-Week, Multicenter, Masked, Randomized Trial (with an 18-Week Masked Extension) to Assess the Safety and Efficacy of 700 µg and 350 µg Dexamethasone Posterior Segment Drug Delivery System (DEX ... | ||
Medical condition: Non-infectious ocular inflammation of the posterior segment in intermediate or posterior uveitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) AT (Completed) IT (Completed) PT (Completed) BE (Completed) CZ (Completed) DE (Completed) GR (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000737-36 | Sponsor Protocol Number: 206207-015 | Start Date*: 2006-05-17 |
Sponsor Name:Allergan Limited | ||
Full Title: A 6-Week, Multicenter, Masked, Randomized Trial (with a 20-Week Masked Extension) to Assess the Safety and Efficacy of 700 µg and 350 µg Dexamethasone Posterior Segment Drug Delivery System (DEX PS... | ||
Medical condition: Non-infectious ocular inflammation of the anterior segment in anterior uveitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) AT (Prematurely Ended) PT (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-016839-35 | Sponsor Protocol Number: PX-171-009 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:Onyx Therapeutics, Inc. | |||||||||||||
Full Title: Estudio en fase 3 multicéntrico y aleatorizado de comparación de carfilzomib, lenalidomida y dexametasona (CRd) con lenalidomida y dexametasona (Rd) en pacientes con mieloma múltiple recidivado. A... | |||||||||||||
Medical condition: Mieloma múltiple. Multiple myeloma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) BE (Completed) NL (Completed) CZ (Completed) DE (Completed) AT (Completed) BG (Completed) FR (Completed) HU (Completed) SE (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001564-19 | Sponsor Protocol Number: CLBH589D2222 | Start Date*: 2016-04-29 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A multicenter, randomized, open-label Phase 2 study evaluating the safety and efficacy of three different regimens of oral panobinostat in combination with subcutaneous bortezomib and oral dexameth... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) SE (Completed) NO (Completed) DE (Completed) NL (Completed) HU (Completed) GR (Completed) PL (Completed) CZ (Completed) PT (Completed) IT (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019820-30 | Sponsor Protocol Number: CC-4047-MM-003 | Start Date*: 2011-03-31 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Open-label Study to Compare the Efficacy and Safety of Pomalidomide in Combination with Low-Dose Dexamethasone versus High-Dose Dexamethasone in Subjects with Re... | |||||||||||||
Medical condition: Refractory Multiple Myeloma (MM) or relapsed and refractory MM. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) DE (Completed) GR (Completed) IT (Completed) CZ (Completed) NL (Completed) ES (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000928-37 | Sponsor Protocol Number: 64007957MMY3006 | Start Date*: 2023-02-15 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3 Randomized Study Comparing Teclistamab Monotherapy versus Pomalidomide, Bortezomib, Dexamethasone (PVd) or Carfilzomib, Dexamethasone (Kd) in Participants with Relapsed or Refractory Mult... | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) FR (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) NL (Trial now transitioned) DK (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) CZ (Trial now transitioned) GR (Trial now transitioned) AT (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000105-73 | Sponsor Protocol Number: OPTIMAL | Start Date*: 2019-05-22 | |||||||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||||||||||||
Full Title: Efficacy of metfOrmin in PrevenTIng glucocorticoid-induced diabetes in Melanoma, breAst or Lung cancer patients with brain metastases: the phase II OPTIMAL study | |||||||||||||||||||||||
Medical condition: Patients with melanoma, lung or breast cancer with encephalic metastases. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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