- Trials with a EudraCT protocol (162)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
162 result(s) found for: Tissue Repair.
Displaying page 1 of 9.
EudraCT Number: 2019-004939-24 | Sponsor Protocol Number: BPF-001 | Start Date*: 2020-06-02 | |||||||||||
Sponsor Name:Cell and Gene Therapy Catapult | |||||||||||||
Full Title: Phase I/II open-label study to assess the safety, tolerability and efficacy of a novel tissue engineered airway product, consisting of expanded autologous bone marrow (BM) derived Mesenchymal Strom... | |||||||||||||
Medical condition: Bronchopleural fistula (BPF) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003461-41 | Sponsor Protocol Number: HP4.3 | Start Date*: 2007-11-13 |
Sponsor Name:Deutsche Herzzentrum Berlin, Kompetenznetz Angeborene Herzfehler | ||
Full Title: Cardiac imaging under dobutamine stress for early assessment of right ventricular function in patients with tetralogy of Fallot and pulmonary regurgitation | ||
Medical condition: Fallot tetralogy late after repair with marked pulmonary valve incompetence | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003674-32 | Sponsor Protocol Number: 1.1:12-6-2015 | Start Date*: 2016-02-23 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of Telmisartan on inflammatory processes in the vascular wall of abdominal aortic aneurysms. | ||
Medical condition: Abdominal aortic aneurysm with an indication for elective open surgical repair. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001286-42 | Sponsor Protocol Number: ABI 55-0603-1 | Start Date*: 2006-09-20 |
Sponsor Name:Aastrom Biosciences, Inc | ||
Full Title: Multi-center, Multi-national Clinical Trial of the Application of Tissue Repair Cell (TRC) Therapy of Osteonecrosis in the Femur Head | ||
Medical condition: Osteonecrosis of the femur head | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005798-22 | Sponsor Protocol Number: AAG-G-H-1202 | Start Date*: 2012-11-05 | ||||||||||||||||||||||||||
Sponsor Name:TETEC – Tissue Engineering Technologies – AG | ||||||||||||||||||||||||||||
Full Title: A Clinical Study to Evaluate the Safety and Effectiveness of NOVOCART® 3D plus Compared to Microfracture in the Treatment of Articular Cartilage Defects of the Knee. | ||||||||||||||||||||||||||||
Medical condition: Repair of localized, full-thickness cartilage defects of the femoral condyle (medial, lateral or trochlea) of 2-6cm². | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) HU (Completed) LV (Completed) LT (Completed) FR (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: (No results available) |
EudraCT Number: 2015-005162-34 | Sponsor Protocol Number: clinical_study_protocol | Start Date*: 2017-05-19 | |||||||||||
Sponsor Name:University Hospital Basel | |||||||||||||
Full Title: Randomized, multi-center phase II clinical trial for the regeneration of cartilage lesions in the knee using nasal chondrocyte-based tissue (NTEC) or nasal chondrocyte-based cell (N-CAM)-therapies | |||||||||||||
Medical condition: Patients must display 1-2 symptomatic, focal cartilage lesion grade IIIIV (according to the grading by the International Cartilage Repair Society (ICRS)) from 2 to 8 cm2 on the femoral condyle and/... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000589-31 | Sponsor Protocol Number: NEMESIS | Start Date*: 2018-02-02 | ||||||||||||||||
Sponsor Name:SOCIETà CAMPANA DI IMMUNOTERAPIA ONCOLOGICA | ||||||||||||||||||
Full Title: multi stage phase II trial of Nivolumab (an anti –PD-1) in patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
Medical condition: patients with platinum resistant Mismatch Repair deficient germinal cells tumours | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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: 2008-001732-13 | Sponsor Protocol Number: SPIO_180308 | Start Date*: 2008-09-03 |
Sponsor Name:University of Edinburgh | ||
Full Title: Magnetic Resonance Imaging of Aortic Aneurysm Instability | ||
Medical condition: Abdominal Aortic Aneurysm disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001755-38 | Sponsor Protocol Number: J32B11JM54 | Start Date*: 2005-11-04 |
Sponsor Name:Fundación Teknon | ||
Full Title: Clinical Trial phase I-II, Multicentic of the Application of TRC in the Surgical Treatment of Non-Hypertrophic Pseudoarthrosis and Complex Fractures of Long Bones Ensayo Clínico Fase I-II, multicén... | ||
Medical condition: Surgical Treatment of Non-Hypertrophic Pseudoarthrosis and Complex Fractures of Long Bones | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003418-28 | Sponsor Protocol Number: CLNA043X2201 | Start Date*: 2017-04-18 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, patient and investigator blinded, single dose, Proof of Concept study investigating the safety, tolerability and preliminary efficacy of intra-articular LNA043 in ... | |||||||||||||
Medical condition: Acute cartilage injuries | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002036-32 | Sponsor Protocol Number: C3441006(MDV3800-06) | Start Date*: 2016-12-05 | ||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||
Full Title: TALAPRO 1: A PHASE 2, OPEN LABEL, RESPONSE RATE STUDY OF TALAZOPARIB IN MEN WITH DNA REPAIR DEFECTS AND METASTATIC CASTRATION RESISTANT PROSTATE CANCER WHO PREVIOUSLY RECEIVED TAXANE BASED CHEMOTHE... | ||||||||||||||||||
Medical condition: Men With DNA Repair Defects and Metastatic Castration-Resistant Prostate Cancer Who Previously Received Taxane-Based Chemotherapy and Progressed on at Least 1 Novel Hormonal Agent (Enzalutamide and... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) ES (Ongoing) FR (Completed) BE (Ongoing) GB (Completed) AT (Completed) DK (Prematurely Ended) HU (Completed) IT (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002057-38 | Sponsor Protocol Number: 64091742PCR2001 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 2 Efficacy and Safety Study of Niraparib in Men with Metastatic Castration-Resistant Prostate Cancer and DNA-Repair Anomalies | |||||||||||||
Medical condition: mCRPC and DNA-repair anomalies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) BE (Completed) DK (Prematurely Ended) NL (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002209-25 | Sponsor Protocol Number: 67652000PCR3002 | Start Date*: 2020-10-12 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3 Randomized, Placebo-controlled, Double-blind Study of Niraparib in Combination with Abiraterone Acetate and Prednisone Versus Abiraterone Acetate and Prednisone for the Treatment of Parti... | |||||||||||||
Medical condition: Deleterious Germline or Somatic Homologous Recombination Repair (HRR) Gene-Mutated Metastatic Castration-Sensitive Prostate Cancer (mCSPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Trial now transitioned) FR (Trial now transitioned) CZ (Trial now transitioned) HU (Trial now transitioned) BE (Trial now transitioned) NL (Ongoing) DK (Trial now transitioned) PL (Trial now transitioned) DE (Ongoing) PT (Ongoing) BG (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002653-23 | Sponsor Protocol Number: 1/07 | Start Date*: 2008-09-02 | |||||||||||
Sponsor Name:The Police Rehabilitation Centre, Flint House | |||||||||||||
Full Title: A pilot for a case control study to evaluate the effects of High Dosage Oxygen Therapy as an adjunct to an established program of physiotherapy and rehabilitation for sub acute soft tissue knee con... | |||||||||||||
Medical condition: Sub acute soft tissue injuries to the knee . | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000421-21 | Sponsor Protocol Number: CROCIATO | Start Date*: 2007-02-20 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: PROSPECTIVE, RANDOMIZED, DUOBLE BLIND COMPARISON BETWEEN SUBARACNOID ANAESTHESIA AND SUBARACNOID ANAESTHESIA WITH BLOCK OF FEMORAL NERVE IN PATIENTS UNDERGOING SURGERY FOR ANTERIOR LIGAMENT REPAIR. | |||||||||||||
Medical condition: PATIENTS UNDERGOING SURGERY FOR CRUSADER ANTERIOR LIGAMENT | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002344-99 | Sponsor Protocol Number: SKY0402-C-203 | Start Date*: 2005-03-03 | |||||||||||
Sponsor Name:SkyePharma, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Dose-Escalating/De-Escalating Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Sustained-Release Encapsulated Bupivacaine (SKY0402) ... | |||||||||||||
Medical condition: Pain following bunionectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2009-016970-33 | 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 |
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