- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Dental Material.
Displaying page 1 of 1.
EudraCT Number: 2012-002002-46 | Sponsor Protocol Number: 2012-BMP1-2 | Start Date*: 2013-05-07 | |||||||||||
Sponsor Name:Universitätsklinik für Zahn-, Mund- und Kieferheilkunde, Med Uni Graz, Department für zahnärztliche Chirurgie | |||||||||||||
Full Title: A phase III, randomized, controlled clinical pilot trial of lateral ridge augmentation using autogenous bone blocks or xenogenic bone block grafts loaded with recombinant human bone morphogenic pro... | |||||||||||||
Medical condition: Difference of percepetion/acceptance in patients trated with autogonous bone blocks or xenogenic bone block loaded with BMP2 to create a sufficent bonesituation Difference in quantity and quality... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004564-26 | Sponsor Protocol Number: BAS20 | Start Date*: 2021-09-20 | |||||||||||
Sponsor Name:Karolinska Institute | |||||||||||||
Full Title: Role of antibiotics in conjunction with oral bone augmentation procedures (BAS20) | |||||||||||||
Medical condition: Patients requiring bone augmentation procedure prior to, or in conjunction to installation of dental implants. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001468-21 | Sponsor Protocol Number: KIIOIW001 | Start Date*: 2006-08-24 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Sympthomatic and prophylactic treatment of drug induced oral dryness in elderly patients with high drug consumption. | ||
Medical condition: Oral dryness is a common problem with serious consquences, especially among elderly individuals. The most common reason for oral dryness is drug consumption. Research has shown that an individual w... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005374-26 | Sponsor Protocol Number: ECAELEV21 | Start Date*: 2022-08-18 |
Sponsor Name:OMEQUI coordinator | ||
Full Title: Efficacy of platelet- and leukocyte-rich fibrin (L-PRF) in reducing healing time in sinus lift combined with deproteinized bovine mineralized bone (DBBM): randomized clinical trial. | ||
Medical condition: If the application of L-PRF with respect to the use of DBBM shows that there are differences in the percentage of new bone between the LPRF group and the control group at 4 and 6 months | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003391-37 | Sponsor Protocol Number: Scil-MD05-C01 | Start Date*: 2005-12-05 | |||||||||||
Sponsor Name:Scil Technology GmbH | |||||||||||||
Full Title: Pilot Study on Safety and explorative Efficacy of MD05 in Comparison with the Medical Device Beta-TCP Mixed with Autogenous Bone Material in Patients Undergoing Two-Stage Unilateral Maxillary Sinus... | |||||||||||||
Medical condition: Requirement of two-stage unilateral maxillary sinus floor augmentation in case of insufficient bone height in the area of the posterior maxilla, prior to insertion of dental implants. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002441-12 | Sponsor Protocol Number: 1219 | Start Date*: 2013-12-16 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: A blind randomized multicenter study of accelerated fractionated chemo-radiotherapy with or without the hypoxic radiosensitizer nimorazole (Nimoral), using a 15 gene signature for hypoxia in the tr... | |||||||||||||
Medical condition: Squamous cell carcinoma of the head and neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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