- Trials with a EudraCT protocol (16)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
16 result(s) found for: Osteonecrosis of the jaw.
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EudraCT Number: 2007-007842-36 | Sponsor Protocol Number: DAHANCA-21 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:Lone Elisabeth Forner | |||||||||||||
Full Title: Hyperbaric oxygen treatment of mandibular osteoradionecrosis. A randomized clinical trial. | |||||||||||||
Medical condition: Mandibular osteoradionecrosis occuring from radiation treatment of cancer. No healthy volunteers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002669-13 | Sponsor Protocol Number: 87RI21_0052 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Limoges University Hospital | |||||||||||||
Full Title: The PENTO protocol in Medication-related osteonecrosis of the jaw (MRONJ): a single-center phase IIa trial | |||||||||||||
Medical condition: Medication-related osteonecrosis of the jaw (MRONJ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006225-27 | Sponsor Protocol Number: SP000283 | Start Date*: 2008-12-15 | |||||||||||
Sponsor Name:The University of Liverpool [...] | |||||||||||||
Full Title: Hyperbaric Oxygen to Prevent Osteoradionecrosis of the Irradiated Mandible (HOPON) | |||||||||||||
Medical condition: Osteoradionecrosis (ORN) of the irradiated mandible; the most feared complication of radiotherapy for head and neck cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000887-32 | Sponsor Protocol Number: ORN-02 | Start Date*: 2015-07-20 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen/NÄL | ||||||||||||||||||
Full Title: Prophylactic treatment of osteoradionecrosis (ORN) with pentoxifylline and α-tocopherol (PENTO) | ||||||||||||||||||
Medical condition: Osteoradionecrosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000618-23 | Sponsor Protocol Number: ORN-01 | Start Date*: 2015-05-05 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen/NÄL | ||||||||||||||||||
Full Title: Treatment of osteoradionecrosis (ORN) with pentoxifylline and α-tocopherol (PENTO) | ||||||||||||||||||
Medical condition: Osteoradionecrosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002096-17 | Sponsor Protocol Number: EORTC-1762-STBSG | Start Date*: 2020-04-21 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | |||||||||||||
Full Title: Reduced dose-density of denosumab for maintenance therapy of unresectable giant cell tumor of bone: a multicenter phase II study "REDUCE" | |||||||||||||
Medical condition: Giant cell tumor of bone | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) DK (Completed) ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001492-37 | Sponsor Protocol Number: Z-AMD | Start Date*: 2019-11-01 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Zoledronic acid as adjuvant therapy in neovascular Age-related Macular Degeneration (The Z-AMD study): a randomized controlled pilot study | |||||||||||||
Medical condition: Neovascular Age-related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002678-11 | Sponsor Protocol Number: ICO-13-001 | Start Date*: 2018-06-07 |
Sponsor Name:Institut Català d’Oncologia | ||
Full Title: An open label biomarker pilot study of the antitumoral acrivity of denosumab in the pre-operative setting of early breast cancer | ||
Medical condition: early breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2012-002107-17 | Sponsor Protocol Number: RG_11-152 | Start Date*: 2013-02-01 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: International Randomised Controlled Trial for the Treatment of Newly Diagnosed Ewing's Sarcoma Family of Tumours | |||||||||||||
Medical condition: Ewing's Sarcoma Family of Tumours | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) BE (Completed) CZ (Completed) IE (Completed) HU (Completed) NL (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001189-87 | Sponsor Protocol Number: SAKK96/12 | Start Date*: 2017-07-18 | ||||||||||||||||
Sponsor Name:Swiss Group for Clinical Cancer Research | ||||||||||||||||||
Full Title: Prevention of Symptomatic Skeletal Events with Denosumab Administered every 4 Weeks versus every 12 Weeks - A Non-Inferiority Phase III trial | ||||||||||||||||||
Medical condition: Bone metastases from castration resistant prostate cancer or from breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003609-24 | Sponsor Protocol Number: MB09-C-01-19 | Start Date*: 2021-12-30 | |||||||||||
Sponsor Name:mAbxience Research S.L. | |||||||||||||
Full Title: A randomised, double-blind, parallel, multicentre, multinational study to compare the efficacy, pharmacokinetics, pharmacodynamics, safety and immunogenicity of MB09 (proposed denosumab biosimilar)... | |||||||||||||
Medical condition: Postmenopausal women diagnosed with osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: EE (Completed) BG (Completed) PL (Completed) LV (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005244-42 | Sponsor Protocol Number: 20159990 | Start Date*: 2018-06-04 | |||||||||||||||||||||||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||||||||||||
Full Title: An Open-label, Multi-center, Phase 2 Study of Denosumab in Subjects with Giant Cell Rich Tumors of Bone. | |||||||||||||||||||||||||||||||||
Medical condition: Aneurysmal bone cysts, giant cell granuloma, other giant cell rich lesions (primary bone, non-malignant) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) FR (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003264-38 | Sponsor Protocol Number: ML18508 | Start Date*: 2005-12-15 | |||||||||||
Sponsor Name:Roche Pharma AG | |||||||||||||
Full Title: COMPARE: Comparison Ibandronate - Zoledronate regarding nephrotoxicity in patients with multiple myeloma | |||||||||||||
Medical condition: Patients with confirmed multiple myeloma stage II-III according to Salmon and Durie, where treatment with bisphosphonate is indicated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002187-49 | Sponsor Protocol Number: EB-CLIN-1001-03 | Start Date*: 2021-08-16 | |||||||||||
Sponsor Name:Eden Biologics, Inc., Taiwan | |||||||||||||
Full Title: A Multinational, Randomized, Double-Blind, Active-Controlled Phase 3 Study to Compare the Clinical Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of EB1001 Biosimilar With EU-Licensed Pro... | |||||||||||||
Medical condition: Osteoporosis is a disorder of impaired bone strength that results in skeletal fragility and increased fracture risk. It is a common and costly disorder, and is associated with significant morbidity... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) EE (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003985-40 | Sponsor Protocol Number: CZOL446G2422 | Start Date*: 2006-01-09 |
Sponsor Name:Department of Internal Medicine, University Hospital Gasthuisberg | ||
Full Title: A prospective multicentre phase II trial of zoledronic acid in patients with myelofibrosis with myeloid metaplasia (MMM) | ||
Medical condition: myelofibrosis with myeloid metaplasia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Completed) DE (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001526-26 | Sponsor Protocol Number: 083 | Start Date*: 2013-10-23 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: An Observational Follow-Up Study for: A Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Odanacatib (MK-0822) to Reduce the Risk of Fracture in Osteoporo... | |||||||||||||
Medical condition: Osteoporosis | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) LT (Completed) DE (Completed) EE (Completed) LV (Completed) ES (Completed) CZ (Completed) PL (Completed) BG (Completed) DK (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
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