- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
25 result(s) found for: Bone remodeling.
Displaying page 1 of 2.
EudraCT Number: 2021-005401-28 | Sponsor Protocol Number: AOI2021ME_PICKERING | Start Date*: 2022-01-26 |
Sponsor Name:University Hospital of Clermont-Ferrand | ||
Full Title: Effects of the combination of magnesium bisphosphonates versus bisphosphonates alone on bone remodeling: Randomized pilot clinical trial | ||
Medical condition: postmenopausal osteoporosis | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000925-71 | Sponsor Protocol Number: HUM 05-032 | Start Date*: 2006-04-27 |
Sponsor Name:University Hospital Ghent | ||
Full Title: TNF-blockade for the treatment of erosive osteoarthritis (OA) of interphalangeal finger joints. Randomized, double blind, placebo-controlled study to evaluate the efficacy of adalimumab 40 mg sc ev... | ||
Medical condition: Erosive interphalangeal osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005511-32 | Sponsor Protocol Number: XEOLAS | Start Date*: 2022-09-12 |
Sponsor Name:Xeolas Pharmaceuticals Ltd. | ||
Full Title: A Randomized Control Trial Phase (IIIa) Unicentric, Placebo Controlled, Double-Blinded Study to confirm the Efficacy and Safety of “Effects of topical Alendronic Acid on alveolar bone remodeling af... | ||
Medical condition: Healthy patients periodontal disease, that qualify for oral surgery of the alveolar bone(ASA I and II) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002965-19 | Sponsor Protocol Number: 1 | Start Date*: 2005-03-14 |
Sponsor Name:Orthopaedic department, Karolinska Institutet, Danderyd's Hospital | ||
Full Title: Can risedronate prevent periprosthetic bone loss after hip arthroplasty? A randomized, double-blind, placebo-controlled trial | ||
Medical condition: Periprosthetic bone loss after total hip arthroplasty (THA) is the main factor in limiting the longevity of implants used för treatment of osteoarthritis. Bone loss leads to implant destabilization... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000774-46 | Sponsor Protocol Number: BOOST-2 | Start Date*: 2005-08-18 |
Sponsor Name:Medical School, Dept. of Cardiology and Angiology | ||
Full Title: BOne marrOw transfer to enhance ST-elevation infarct regeneration-2 | ||
Medical condition: Patients with coronary artery disease, suffering from a large myocardial infarction. The loss of viable myocardium initiates a process of adverse left ventricular (LV) remodeling leading to chambe... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001650-26 | Sponsor Protocol Number: ZOL6700 | Start Date*: 2019-10-25 |
Sponsor Name:Hospital South West Jutland | ||
Full Title: Zoledronic acid for prevention of bone loss after bariatric surgery | ||
Medical condition: Morbid obese subjects undergoing bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005862-38 | Sponsor Protocol Number: | Start Date*: 2007-04-05 |
Sponsor Name:UCL Mont Godinne | ||
Full Title: Prevention of Postmenopausal Bone Loss in Osteopenic Women with Alendronate given on a 70 mg Once-every two week Regimen : a 2-year, Double-blind, Placebo-controlled Clinical Trial | ||
Medical condition: osteopenia and postmenopausal patient | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001848-35 | Sponsor Protocol Number: APB-MET-2017-01 | Start Date*: 2017-12-14 |
Sponsor Name:Juan Blanco Carrion | ||
Full Title: METRONIDAZOLE AS AN ADJUNCT OF NON-SURGICAL TREATMENT OF PERI-IMPLANTITIS: A 6-MONTHS PLACEBO-CONTROLLED CLINICAL TRIAL IN HUMANS. | ||
Medical condition: Peri-implantitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005709-50 | Sponsor Protocol Number: 1122005 | Start Date*: 2006-05-05 |
Sponsor Name:Cardiology, University of Frankfurt | ||
Full Title: Extracorporal shock wave therapy for induction of therapeutic neovascularization and homing of bone marrow progenitor cells in patients with chronic ischemic heart disease | ||
Medical condition: Patients with ischemic coronary artery disease (congestive heart failure) and s/p anterior myocardial infarction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004874-14 | Sponsor Protocol Number: 2007-08-16 REPAIR-ACS | Start Date*: 2008-06-09 |
Sponsor Name:Cardiology, J. W. Goethe University Frankfurt | ||
Full Title: Doppel-blinde, randomisierte, kontrollierte Studie zur Erfassung des Effektes einer intrakoronaren Applikation von Knochenmark-Progenitorzellen auf die koronare Flußreserve bei Patienten mit akutem... | ||
Medical condition: Patients with acute coronary syndrome (NSTEMI) due to coronary artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000931-18 | Sponsor Protocol Number: EL-THOS-001 | Start Date*: 2014-05-27 |
Sponsor Name:Ersi Voskaridou-Dimoula | ||
Full Title: EVALUATION OF EFFICACY OF DENOSUMAB IN PATIENTS WITH THALASSEMIA MAJOR AND OSTEOPOROSIS: A RANDOMIZED, PLACEBO-CONTROLLED, SINGLE-SITE, DOUBLE BLIND PHASE 2B CLINICAL TRIAL | ||
Medical condition: Adult patients with Thalassemia major and osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001282-12 | Sponsor Protocol Number: NVD003-CLN02-CPT | Start Date*: 2022-08-02 |
Sponsor Name:Novadip Biosciences | ||
Full Title: A proof-of-concept study with NVD-003, an autologous osteogenic bone graft, in the treatment of congenital pseudarthrosis of the tibia in pediatric patients | ||
Medical condition: congenital pseudarthrosis of the tibia (CPT) | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000515-95 | Sponsor Protocol Number: B3D-EW-GHCX | Start Date*: 2005-06-16 |
Sponsor Name:Eli Lilly and Company Limited | ||
Full Title: Differential Effects of Teriparatide and Strontium Ranelate on Bone Remodeling and Formation in Postmenopausal Women with Osteoporosis: A Histomorphometric Study | ||
Medical condition: Osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: CZ (Completed) ES (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004347-12 | Sponsor Protocol Number: ICT-10 | Start Date*: 2016-03-05 | |||||||||||
Sponsor Name:Hybrigenics SA | |||||||||||||
Full Title: Exploratory Study of Inecalcitol in Imatinib-Treated Residual Chronic Myeloid Leukaemia: INIM Study | |||||||||||||
Medical condition: Residual disease in Chronic Myeloid Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005529-11 | Sponsor Protocol Number: UX023-CL303 | Start Date*: 2016-02-01 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study with Open-Label Extension to Assess the Efficacy and Safety of KRN23 in Adults with X-linked Hypophosphatemia (XLH) | |||||||||||||
Medical condition: XLH is a disorder of hypophosphatemia, renal phosphate wasting, and the most common inheritable form of rickets. In XLH patients, excess circulating fibroblast growth factor (FGF23) impair phospha... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) FR (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001831-23 | Sponsor Protocol Number: 3100N7-210 WW | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2/3, Multicenter, Double-Blind, Randomized, Controlled Study of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP 2)/Calcium Phosphate Matrix (CPM) in Closed Diaphyseal Tibial Fractures | |||||||||||||
Medical condition: Closed diaphyseal tibial fracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) DE (Prematurely Ended) FI (Completed) GB (Completed) LV (Completed) SI (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001775-41 | Sponsor Protocol Number: UX023-CL304 | Start Date*: 2015-12-16 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
Full Title: An Open-Label, Single-Arm, Phase 3 Study to Evaluate the Effects of KRN23 on Osteomalacia in Adults with X-linked Hypophosphatemia (XLH) | |||||||||||||
Medical condition: XLH is a disorder of hypophosphatemia, renal phosphate wasting, and the most common inheritable form of rickets. In XLH patients, excess circulating fibroblast growth factor (FGF23) impair phospha... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001933-16 | Sponsor Protocol Number: 26866138PCR2002 | Start Date*: 2007-03-13 |
Sponsor Name:Christos N. Papandreou | ||
Full Title: "A Phase II, Open-Label study of Velcade(Bortezomib)for patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy" | ||
Medical condition: Treatment of patients with Androgen-Independent Prostate Carcinoma who progressed on or after prior chemotherapy. | ||
Disease: | ||
Population Age: | Gender: Male | |
Trial protocol: GR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004819-37 | Sponsor Protocol Number: APART_2014 | Start Date*: 2015-04-16 | |||||||||||
Sponsor Name:University College Dublin | |||||||||||||
Full Title: A multi-centre, prospective, randomised trial of short course alendronate therapy or placebo combined with vitamin D and calcium to prevent loss of bone mineral density in antiretroviral-naïve, HIV... | |||||||||||||
Medical condition: Human immunodeficiency virus (HIV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) DK (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002126-36 | Sponsor Protocol Number: BP39261 | Start Date*: 2017-03-01 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center, three-part phase II study to evaluate the safety and efficacy of RO7123520 as adjunct treatment in patients with moderately to severely... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
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