- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Titanium.
Displaying page 1 of 1.
| EudraCT Number: 2007-000911-27 | Sponsor Protocol Number: V00096 CR 205 (ORF) | Start Date*: 2007-09-03 |
| Sponsor Name:ORFAGEN | ||
| Full Title: Evaluation of the protection activity of microfine Ti02, pigmentary Ti02 and bisoctrizole and their combinations in voluntary patients with idiopathic solar urticaria (SU): phase II photoprovocatio... | ||
| Medical condition: Idiopathic Solar Urticaria (SU) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-002678-19 | Sponsor Protocol Number: SP148MP201 | Start Date*: 2018-03-20 | |||||||||||
| Sponsor Name:SmartPractice | |||||||||||||
| Full Title: Clinical Evaluation of Metal Panel Allergens: Aluminum, Copper, Manganese, Molybdenum, Tin, Titanium, Vanadium and Zinc Dose Response Study | |||||||||||||
| Medical condition: Metal induced contact dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002325-31 | Sponsor Protocol Number: 11.105 | Start Date*: 2005-11-04 |
| Sponsor Name:Taunton & Somerset NHS Trust | ||
| Full Title: Two parallel trials to compare the effectiveness, and potential adverse side-effects, of four routinely used topical therapies to prolong breastfeeding, by either (1) preventing or (2) treating nip... | ||
| Medical condition: Nipple pain in breastfeeding women | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001241-14 | Sponsor Protocol Number: V00096 CR 201 | Start Date*: 2004-11-12 |
| Sponsor Name:Pierre Fabre Dermatologie represented by Institut de Recherche Pierre Fabre | ||
| Full Title: Efficacy of topic RV3131A-HC3221 in the prevention of polymorphic light eruption | ||
| Medical condition: Polymorphic Light Eruption (PMLE) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) DE (Completed) GB (Completed) SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004825-42 | Sponsor Protocol Number: Notapplicablenow | Start Date*: 2016-12-22 |
| Sponsor Name:ACTA | ||
| Full Title: Effect of Delmopinol on treatment of Peri - implant mucositis : a randomised controlled clinical trial | ||
| Medical condition: Peri implant mucositis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001227-39 | Sponsor Protocol Number: 779322 | Start Date*: 2019-12-11 | |||||||||||
| Sponsor Name:University of Bergen, Faculty of Medicin, Department of Clinical Dentistry | |||||||||||||
| Full Title: A randomized controlled clinical trial to assess the efficacy of a combination of autologous mesenchymal stem cells and biomaterial in jaw bone regeneration prior to dental implant placement in com... | |||||||||||||
| Medical condition: Patients in need of dental implant(s) in the upper and lower jaws with presence of bone defects with loss in vertical height and < than 4 mm in lateral width | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) NO (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004940-48 | Sponsor Protocol Number: 2013-004940-48 | Start Date*: 2014-11-12 |
| Sponsor Name:Danderyds Hospital, Department of Clinical Sciences, Division of Orthopaedics | ||
| Full Title: Denosumab For Treating Periprosthetic Osteolysis After Uncemented Total Hip Arthroplasty. A randomized, double-blind, placebo-controlled trial using volumetric computed tomography. | ||
| Medical condition: Patients with titanium press-fit acetabular components with polyethylene liners will be screened for osteolytic lesions. The patients had primary surgery at least 7 years before screening and all o... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004046-15 | Sponsor Protocol Number: TKA4 | Start Date*: 2013-07-03 | |||||||||||
| Sponsor Name:ORtopædkirurgisk Forskningsenhed, Aarhus Universitetshospital | |||||||||||||
| Full Title: A 4-way randomized double-blinded migration (RSA), bone density (DXA), and biomarker study assessing adaptive bone changes and implant fixation and longevity of the new Regenerex Porous Titanium Ti... | |||||||||||||
| Medical condition: Osteoarthritis in the knee treated with cementless total knee arthroplasty | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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