- Trials with a EudraCT protocol (832)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (124)
832 result(s) found for: Dexamethasone.
Displaying page 1 of 42.
EudraCT Number: 2005-006018-16 | Sponsor Protocol Number: | Start Date*: 2006-02-27 |
Sponsor Name:Royal Marsden Hospital | ||
Full Title: A Randomised Phase III Trial Of Low Dose DailyDexamethasone Versus Intermittent Dexamethasone Versus Prednisolone In Hormone Refractory Prostate Cancer | ||
Medical condition: Hormone refractory prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001341-41 | Sponsor Protocol Number: RBHP-2016-CONSTANTIN | Start Date*: 2016-07-01 |
Sponsor Name:CHU de Clermont-Ferrand | ||
Full Title: . | ||
Medical condition: . | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000615-25 | Sponsor Protocol Number: C-07-13 | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Efficacy Evaluation of Topical Moxidex Otic Solution in the Treatment of Acute Otitis Externa | |||||||||||||
Medical condition: Acute Otitis Externa | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000242-18 | Sponsor Protocol Number: DEXSAR-Trial | Start Date*: 2013-05-23 |
Sponsor Name: | ||
Full Title: Low dose dexamethasone in newly diagnosed sarcoidosis | ||
Medical condition: Patients with newly diagnosed, pulmonary sarcoidosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002081-20 | Sponsor Protocol Number: 2010_52 | Start Date*: 2013-05-13 |
Sponsor Name:CENTRE HOSPITALIER UNIVERSITAIRE DE LILLE | ||
Full Title: A Multicenter Open label Phase II study of Pomalidomide and Dexamethasone in Progressive Relapsed or Refractory Multiple Myeloma patients with deletion 17p or translocation (4;14) Adverse Karyotypi... | ||
Medical condition: This study will determine the efficacy and toxicity profile of pomalidomide and dexamethasone in patients with adverse prognostic factors as determined using adverse karyotypic abnormalities and th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004566-14 | Sponsor Protocol Number: SanteonCAP | Start Date*: 2012-01-09 |
Sponsor Name: | ||
Full Title: Santeon-CAP study Dexamethasone in community-acquired pneumonia. | ||
Medical condition: Patients with a community-acquired pneumonia who are admitted to the hospital. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004983-23 | Sponsor Protocol Number: 201900874 | Start Date*: 2021-01-18 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Bioequivalence study of prednisolone and dexamethasone: corticosteroids revisited | ||
Medical condition: This study does not investigate a medical condition and is performed in healthy volunteers. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022894-32 | Sponsor Protocol Number: RG_10-209 | Start Date*: 2011-02-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Dexamethasone Reduces Emesis After Major gastrointestinal Surgery (DREAMS trial) - A prospective, double-blind, multicentre, randomised control trial | ||
Medical condition: Patients undergoing nausea and vomiting following elective colorectal resections | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003705-17 | Sponsor Protocol Number: LUMC-NECH-201801-ACA | Start Date*: 2019-03-22 |
Sponsor Name:LUMC | ||
Full Title: Prevention of neuropsychiatric adverse effects caused by dexamethasone: translational insights from a placebo-controlled trial with hydrocortisone. | ||
Medical condition: Neuropsychiatric adverse effects which can be caused by dexamethasone. For example delirium, anxiety, depression, mania and psychosis. But also cognitive impairment and sleep disturbance. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000286-36 | Sponsor Protocol Number: LEVODESA_04-2017 | Start Date*: 2018-08-28 | |||||||||||
Sponsor Name:NTC s.r.l. | |||||||||||||
Full Title: An international, multicenter, randomized, blinded-assessor, parallel-group clinical study comparing eye drops of combined LEvofloxAcin + DExamethasone foR 7 days followed by dexamethasone alone fo... | |||||||||||||
Medical condition: Prevention and treatment of inflammation and prevention of infection associated with cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020174-42 | Sponsor Protocol Number: ZonMw11510009 | Start Date*: 2011-11-04 |
Sponsor Name:ZonMw | ||
Full Title: Dexamethasone for the prevention of a pain flare after palliative radiotherapy for painful bone metastases: a multicenter double-blind placebo-controlled randomized study | ||
Medical condition: Bone metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005565-12 | Sponsor Protocol Number: MD01 | Start Date*: 2013-02-18 |
Sponsor Name:AZ Groeninge | ||
Full Title: The effect of low dose intravenous dexamethasone on the analgesic duration of single shot interscalene block with ropivacaine for shoulder surgery. A prospective, double blind, randomized, placebo ... | ||
Medical condition: Postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001349-41 | Sponsor Protocol Number: MD2012/1 | Start Date*: 2012-05-15 |
Sponsor Name:AZ Groeninge | ||
Full Title: Influence of dexamethasone on postoperative analgesia after combined spinal epidural for cesarean delivery. | ||
Medical condition: Postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002738-22 | Sponsor Protocol Number: 62388 | Start Date*: 2018-03-02 | |||||||||||
Sponsor Name:Princess Máxima Center of Pediatric Oncology | |||||||||||||
Full Title: Double blind placebo controlled randomized intervention study to validate the beneficial effect of hydrocortisone on dexamethasone-induced neurobehavioral side effects in pediatric acute lymphoblas... | |||||||||||||
Medical condition: Acute lymphoblastic leukemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001355-76 | Sponsor Protocol Number: UCL/13/0291 | Start Date*: 2016-05-09 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Phase III randomised trial of immunomodulatory therapy in high risk solitary bone plasmacytoma | |||||||||||||
Medical condition: Solitary bone plasmacytoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003405-98 | Sponsor Protocol Number: dexFEMv2 | Start Date*: 2012-12-03 | |||||||||||
Sponsor Name:ACCORD University of Edinburgh [...] | |||||||||||||
Full Title: Developmental Clinical Studies - Reversing endometrial glucocorticoid deficiency in heavy menstrual bleeding | |||||||||||||
Medical condition: Endometrial glucocorticoid deficiency in Heavy Menstrual Bleeding | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003097-41 | Sponsor Protocol Number: EFC14335 | Start Date*: 2017-02-20 | |||||||||||
Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Phase 3 Randomized, Open-label, Multicenter Study Comparing Isatuximab (SAR650984) in Combination with Pomalidomide and Low-dose Dexamethasone versus Pomalidomide and Low-dose Dexamethasone in Pa... | |||||||||||||
Medical condition: Haematological malignancy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) PT (Completed) ES (Completed) CZ (Ongoing) GB (GB - no longer in EU/EEA) SK (Completed) BE (Completed) DK (Completed) FR (Ongoing) GR (Completed) DE (Completed) PL (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000428-15 | Sponsor Protocol Number: STEROID | Start Date*: 2006-04-19 |
Sponsor Name:HANNA THORÉN | ||
Full Title: INFLUENCE OF DEKSAMETASONE ON POST-OPERATIVE RECOVERY AFTER OPERATIVE TREATMENT OF FACIAL FRACTURES | ||
Medical condition: FRACTURES OF THE FACIAL BONES | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001170-92 | Sponsor Protocol Number: 16787 | Start Date*: 2007-09-12 |
Sponsor Name:Erasmus MC | ||
Full Title: Dexamethasone for postoperative pain relief following tonsillectomy in children | ||
Medical condition: (Adeno)Tonsillectomy and Pain | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018486-37 | Sponsor Protocol Number: dexa2010 | Start Date*: 2010-05-21 |
Sponsor Name:Kris-och Traumacentrum | ||
Full Title: Treatment of exacerbations of post-traumatic stress disorder by short-term dexamethasone, a pilot study. | ||
Medical condition: Posttraumatic stress syndrome F431 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
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