- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Fibula Fracture.
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EudraCT Number: 2015-000650-38 | Sponsor Protocol Number: ALLOB-MF1 | Start Date*: 2015-07-01 | |||||||||||
Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
Full Title: A Phase IIA, multicentre, open study on the safety and efficacy of allogeneic osteoblastic cells (ALLOBĀ®) implantation in multiple non-infected delayed-union (DU) fractures | |||||||||||||
Medical condition: Multiple non-infected delayed-union fractures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005333-36 | Sponsor Protocol Number: ALLOB-DU1 | Start Date*: 2013-07-30 | |||||||||||
Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
Full Title: A pilot Phase I/IIa, multicentre, open proof-of-concept study on the efficacy and safety of allogeneic osteoblastic cells (ALLOBĀ®) implantation in non-infected delayed-union fractures | |||||||||||||
Medical condition: Non-infected delayed-union fractures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
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 (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001630-18 | Sponsor Protocol Number: CWL15001 | Start Date*: 2023-09-20 | |||||||||||
Sponsor Name:5med GmbH | |||||||||||||
Full Title: A randomized, parallel group, multi-center study of a fentanyl nasal spray compared with placebo nasal spray for postoperative pain management and prolonged open treatment over up to 120 hours post... | |||||||||||||
Medical condition: Management of pain following orthopedic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
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