- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Chondrocytes.
Displaying page 1 of 1.
EudraCT Number: 2010-022072-31 | Sponsor Protocol Number: R5242A789 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:RJAH Orthopaedic Hospital | |||||||||||||
Full Title: Autologous Cell Therapy for Osteoarthritis: An evaluation of the safety and efficacy of autologous transplantation of articular chondrocytes and/or bone marrow-derived stromal cells to repair chond... | |||||||||||||
Medical condition: osteochondral defects of the knee (early osteoarthritis) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000784-16 | Sponsor Protocol Number: NCPACI | Start Date*: 2016-04-15 |
Sponsor Name:Akershus University Hospital | ||
Full Title: Focal cartilage defects in the knee – A randomized controlled trial comparing Autologous Chondrocyte Implantation with arthroscopic debridement | ||
Medical condition: Symptomatic focal cartilage defects in the knee | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004989-16 | Sponsor Protocol Number: AGO/2011/011 | Start Date*: 2012-03-27 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: The effect of morphine and different local anesthetics on human chondrocytes: an in vivo study. | |||||||||||||
Medical condition: Patients undergoing total knee arthroplasty. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003594-28 | Sponsor Protocol Number: BCCT2011 | Start Date*: 2013-11-07 | ||||||||||||||||
Sponsor Name:BioTissue Technologies GmbH | ||||||||||||||||||
Full Title: A Comparative Observational Prospective Randomized Open-Label Study on Efficacy of BioSeed®-C and chondrotissue® Treatment of Local Femoral Cartilage Defects in the Knee. | ||||||||||||||||||
Medical condition: focal femoral cartilage defects in the knee joint | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001570-29 | Sponsor Protocol Number: NL4014200012 | Start Date*: 2012-08-28 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Instant MSC Product accompanying Autologous Chondron Transplantation (IMPACT) for focal articular cartilage lesions of the knee; feasibility and safety | ||
Medical condition: Articular cartilage defects of the femural condyl and trochlea of the knee | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003481-18 | Sponsor Protocol Number: CART.III. | Start Date*: 2008-11-17 |
Sponsor Name:TBF | ||
Full Title: PHASE III PROTOCOL COMPARING A MICROFRACTURE TREATMENT TO A CARTIPATCH® CHONDROCYTE GRAFT TREATMENT IN FEMORAL CONDYLE LESIONS | ||
Medical condition: Femoral condyles single lesion from trauma or osteochondritis dissequans with invalidant signs | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003584-11 | Sponsor Protocol Number: MACT-IBK-2015 | Start Date*: 2015-12-11 | ||||||||||||||||
Sponsor Name:Medical University Innsbruck | ||||||||||||||||||
Full Title: Matrix-associated autologous chrondrocyte transplantation for grade four cartilage lesions of the knee joint - clinical and radiological outcome in correlation to the initial cell count of the cho... | ||||||||||||||||||
Medical condition: Cartilage lesion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023830-22 | Sponsor Protocol Number: AAG-G-H-1102 | Start Date*: 2012-05-23 | |||||||||||
Sponsor Name:TETEC AG | |||||||||||||
Full Title: NDisc Study: A Prospective Randomized Multicentre Phase I / II Clinical Trial to Evaluate Safety and Efficacy of NOVOCART® Disc plus Autologous Disc Chondrocyte Transplantation (ADCT) in the Treatm... | |||||||||||||
Medical condition: The subject has a disc herniation with back and /or leg pain (radicular pain) and an identification for sequestrectomy according to the guidelines of DGNC and DGOOC. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004817-16 | Sponsor Protocol Number: MACI00206 | Start Date*: 2008-01-23 | ||||||||||||||||
Sponsor Name:Genzyme Europe B.V. | ||||||||||||||||||
Full Title: A Prospective, Randomized, Open-Label, Parallel-Group, Multicenter Study to Demonstrate the Superiority of Matrix-induced Autologous Chondrocyte Implantation (MACI® implant) versus Arthroscopic Mi... | ||||||||||||||||||
Medical condition: Symptomatic Articular Cartilage Defects of the Femoral Condyle including the Trochlea. osteochondritis dissecans lesions that do not require a bone graft. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) CZ (Completed) SE (Completed) NL (Completed) PL (Completed) DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016816-20 | Sponsor Protocol Number: cod16HS14 | Start Date*: 2010-05-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:co.don AG | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Prospective, randomised, open label, multicentre Phase II clinical trial to investigate the efficacy and safety of the treatment of large defects (4-10 cm2) with 3 different doses of the autologous... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Cartilage defects of knee joints, osteochondral defects | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002601-35 | Sponsor Protocol Number: ACT-2017-01 | Start Date*: 2018-07-02 |
Sponsor Name:PrimeCell Advanced Therapy a.s. | ||
Full Title: A Prospective, Randomized, Controlled, Multicenter, Phase II / III, Clinical Study to Evaluate the Effectiveness and Safety of NTC chondrograft® versus the Standard Procedure Arthroscopic Microfrac... | ||
Medical condition: Symptomatic knee articular cartilage defects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016970-33 | Sponsor Protocol Number: MACI00809 | Start Date*: 2011-03-17 | ||||||||||||||||
Sponsor Name:Genzyme Europe BV | ||||||||||||||||||
Full Title: An Extension Protocol for Participants of Genzyme-Sponsored Prospective, Randomized, Open-Label, Parallel-Group, Multicenter Study of Matrix-Induced Autologous Chondrocyte Implantation (MACI® impl... | ||||||||||||||||||
Medical condition: Symptomatic Articular Cartilage Defects of the Femoral Condyle including the Trochlea. Osteochondritis dissecans lesions that do not require a bone graft. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) CZ (Completed) GB (Completed) SE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002817-22 | Sponsor Protocol Number: AAG-G-H-1624 | Start Date*: 2017-02-09 | |||||||||||||||||||||||||||||||
Sponsor Name:TETEC Tissue Engineering Technologies - AG | |||||||||||||||||||||||||||||||||
Full Title: Prospective, Multicenter, Single-arm Phase III Clinical Trial to Evaluate the Efficacy and Safety of NOVOCART® Inject plus in the Treatment of Cartilage Defects of the Knee | |||||||||||||||||||||||||||||||||
Medical condition: Repair of cartilage defects of the knee (medial or lateral femoral condyle or tibial plateau, trochlea or patella) caused by traumatic events or osteochondritis dissecans (defect size is ≥ 4 and ≤... | |||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) CZ (Completed) DE (Completed) PL (Completed) LT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016466-82 | Sponsor Protocol Number: cod16HS13 | Start Date*: 2010-09-01 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:CO.DON AG | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Prospective, randomised, open label, multicentre Phase-III clinical trial to compare the efficacy and safety of the treatment with the autologous chondrocyte transplantation product co.don chondros... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Cartilage defects of knee joints, osteochondral defects | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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