- Trials with a EudraCT protocol (72)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
72 result(s) found for: Dexamethasone sodium phosphate.
Displaying page 1 of 4.
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 (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005008-15 | Sponsor Protocol Number: Okhn1001 | Start Date*: 2006-11-08 | |||||||||||
Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | |||||||||||||
Full Title: Exploratory study of intravitreal clindamycin and dexamethasone in the treatment of acute toxoplasma chorioretinitis associated vitritis | |||||||||||||
Medical condition: Vitritis secondary to acute toxoplasma chorioretinitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004498-29 | Sponsor Protocol Number: 20190360 | Start Date*: 2022-01-13 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: Phase 3 Randomized, Controlled Study of Blinatumomab Alternating With Low-intensity Chemotherapy Versus Standard of Care for Older Adults With Newly Diagnosed Philadelphia-negative B-cell Precursor... | |||||||||||||
Medical condition: Newly Diagnosed Philadelphia (Ph)-negative B-cell Precursor Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PT (Trial now transitioned) SE (Trial now transitioned) AT (Trial now transitioned) FI (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) DK (Trial now transitioned) IT (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) BG (Trial now transitioned) NL (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014827-21 | Sponsor Protocol Number: RD–5103-009-08 | Start Date*: 2010-09-02 |
Sponsor Name:Derby Hospitals NHS Foundation Trust [...] | ||
Full Title: A single centre double blind randomised controlled trial investigating the use of dexamethasone in the treatment of acute tonsillitis. | ||
Medical condition: Acute bacterial tonsillitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004127-79 | Sponsor Protocol Number: STALMANSHUA | Start Date*: 2018-05-09 |
Sponsor Name:UZ Leuven | ||
Full Title: Comparison of treatment with preservative-free versus preserved dexamethasone 0.1% and diclofenac 0.1% eye drops after cataract surgery. | ||
Medical condition: Treatment after cataract surgery | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000200-14 | Sponsor Protocol Number: | Start Date*: 2005-07-08 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: A randomised, double-blinded comparison of the effectiveness of intravenously administered Ketoralac versus Dexamethasone in the treatment of pain following surgical removal of third molar teeth un... | ||
Medical condition: Pain experienced after the surgical removal of impacted third molars. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003953-16 | Sponsor Protocol Number: OTO4008 | Start Date*: 2016-04-05 | |||||||||||
Sponsor Name:ÁREA DE ATENCIÓN INTEGRADA DE ALBACETE | |||||||||||||
Full Title: A Phase IIIb study of the efficacy of dexamethasone in irreversible hearing loss prevention in subjects with Ototoxic Oncological Treatment. Otoprotection in cancer treatment. | |||||||||||||
Medical condition: Cisplatin ototoxicity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005137-32 | Sponsor Protocol Number: 14-097 | Start Date*: 2016-10-12 |
Sponsor Name:ENCELADUS Pharmaceuticals BV | ||
Full Title: A Phase I-IIa, Open label, Multi-Center, Dose Escalating Study to Evaluate the Safety of Intravenous Pegylated Liposomal Dexamethasone Sodium Phosphate (Oncocort) as Monotherapy in Patients with Pr... | ||
Medical condition: Multiple Myeloma is a plasma cell malignancy that is characterized by accumulation of clonal plasma cells, mainly in the bone marrow, leading to clinical manifestations such as anemia, bone destruc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003363-25 | Sponsor Protocol Number: NA | Start Date*: 2020-08-18 | ||||||||||||||||
Sponsor Name:Department of Intensive Care, Rigshospitalet | ||||||||||||||||||
Full Title: Higher vs. Lower Doses of Dexamethasone in Patients with COVID-19 and Severe Hypoxia: the COVID STEROID 2 trial | ||||||||||||||||||
Medical condition: Adult patients with COVID-19 and severe hypoxia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2011-003082-15 | Sponsor Protocol Number: KTB-002 | Start Date*: 2011-09-08 | ||||||||||||||||
Sponsor Name:Karen Toftdahl Bjørnholdt | ||||||||||||||||||
Full Title: High dose dexamethasone for pain following arthroscopic shoulder surgery: A randomised blinded clinical trial. | ||||||||||||||||||
Medical condition: Pain following arthroscopic shoulder surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003121-42 | Sponsor Protocol Number: CHDR1635 | Start Date*: 2019-11-28 | |||||||||||
Sponsor Name:Enceladus Pharmaceuticals BV | |||||||||||||
Full Title: A Phase I-IIa, Open label, Dose Escalating Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of Intravenous Pegylated Liposomal Dexamethasone Sodium Phosphate as Monotherapy in Pa... | |||||||||||||
Medical condition: Castration resistant prostate cancer with bone metastases. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (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: 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: 2018-000338-36 | Sponsor Protocol Number: IEDAT-03-2018 | Start Date*: 2018-05-31 | |||||||||||
Sponsor Name:EryDel S.p.A. | |||||||||||||
Full Title: Open-label, Long-term, Extension Treatment using Intra-Erythrocyte Dexamethasone Sodium Phosphate in Patients with Ataxia Telangiectasia Who Participated in the IEDAT-02-2015 Study | |||||||||||||
Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) PL (Completed) GB (GB - no longer in EU/EEA) NO (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002101-23 | Sponsor Protocol Number: 25-03-05 Version 4 | Start Date*: 2006-02-28 |
Sponsor Name:North West London Hospitals NHS Trust, R&D Office | ||
Full Title: Do Steroids Provide Additional Benefit Over Pressure Alone In Reducing Oedema And Ecchymosis Following Rhinoplasty? A Randomised, Prospective, Double Blind, Placebo Controlled Clinical Trial | ||
Medical condition: Nasal deformity requiring corrective surgery i.e Rhinoplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002251-13 | Sponsor Protocol Number: 24052016 | Start Date*: 2016-11-09 |
Sponsor Name:Oulu university hospital | ||
Full Title: The effect of intravenous single-dose dexamethasone on pain after total knee replacement surgery. | ||
Medical condition: Patients with arthrosis of knee joint needing operative treatment i.e. arthroplasty of knee. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-005887-70 | Sponsor Protocol Number: REMED | Start Date*: 2021-01-28 |
Sponsor Name:Fakultní nemocnice Brno | ||
Full Title: Effect of dexamethasone in patients with ARDS and COVID-19 – prospective, multi-centre, open-label, parallel-group, randomized controlled trial | ||
Medical condition: Acute respiratory distress syndrome (ARDS) associated with COVID-19 pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001425-48 | Sponsor Protocol Number: BLUEBERRY | Start Date*: 2021-07-07 |
Sponsor Name:Division of Anaesthesiology - Department of Acute Medicine - Geneva Children's Hospital, University Hospitals of Geneva | ||
Full Title: Dexamethasone and postoperative bleeding following tonsillectomy in children | ||
Medical condition: Tonsillectomy/tonsillotomy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-002308-41 | Sponsor Protocol Number: RB12-032 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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