- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
17 result(s) found for: Corneal transplantation.
Displaying page 1 of 1.
EudraCT Number: 2007-007787-25 | Sponsor Protocol Number: RE OC-02/2007 | Start Date*: 2007-12-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE S. MARIA NUOVA | |||||||||||||
Full Title: Use of subconjunctival Bevacizumab (Avastin) in treatment of corneal neovascularization non curable with standard protocols (topical and sistemic steroids). | |||||||||||||
Medical condition: Corneal neovascularization | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002845-23 | Sponsor Protocol Number: CCD-GPLSCD01-03 | Start Date*: 2015-12-16 | |||||||||||
Sponsor Name:Holostem Terapie Avanzate s.r.l. | |||||||||||||
Full Title: Multinational, multicentre, prospective, open-label, uncontrolled clinical trial to assess the efficacy and safety of Autologous Cultivated Limbal Stem Cells Transplantation (ACLSCT) for restoratio... | |||||||||||||
Medical condition: corneal lesions with associated moderate to severe limbal stem cell deficiency due to ocular burns | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) BE (Completed) NL (Ongoing) FR (Completed) PL (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001344-11 | Sponsor Protocol Number: CCD-GPLSCD01-03-FU | Start Date*: 2018-04-11 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: Multinational, multicenter, prospective, long-term safety and efficacy follow-up study after Autologous Cultivated Limbal Stem Cells Transplantation (ACLSCT) for restoration of corneal epithelium i... | |||||||||||||
Medical condition: corneal lesions with associated moderate to severe limbal stem cell deficiency due to ocular burns | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) PL (Completed) FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) NL (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000608-16 | Sponsor Protocol Number: 5466 | Start Date*: 2011-12-21 |
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust [...] | ||
Full Title: To evaluate the safety and effectiveness of human ex vivo expanded autologous limbal stem cells for the treatment of unilateral total limbal stem cell deficiency | ||
Medical condition: unilateral total limbal stem cell deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000523-14 | Sponsor Protocol Number: EI17-00523 | Start Date*: 2021-11-26 | |||||||||||
Sponsor Name:Universidad Miguel Hernandez | |||||||||||||
Full Title: Transplantation of autologous mesenchymal stem cells of adipose origin for the treatment of corneal diseases | |||||||||||||
Medical condition: Corneal Diseases | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000295-16 | Sponsor Protocol Number: LX201-01 | Start Date*: 2007-07-27 | |||||||||||
Sponsor Name:Lux Biosciences, Inc. | |||||||||||||
Full Title: A MULTI-CENTER, PLACEBO-CONTROLLED, RANDOMIZED, PARALLEL-GROUP DOSE-RANGING STUDY TO ASSESS THE EFFICACY AND SAFETY OF LX201 FOR PREVENTION OF CORNEAL ALLOGRAFT REJECTION EPISODES AND GRAFT FAILURE... | |||||||||||||
Medical condition: Patient after penetrating keratoplasty who are at increased immunological risk for corneal allograft rejection episodes and/or graft failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024409-11 | Sponsor Protocol Number: LSC-001 | Start Date*: 2011-08-11 | |||||||||||
Sponsor Name:Scottish National Blood Transfusion Service [...] | |||||||||||||
Full Title: Pilot Clinical Assessment of Ex Vivo Expanded Corneal Limbal Stem Cell Transplantation in Patients with Severe Ocular Surface Disease (OSD) Arising from Limbal Stem Cell Deficiency | |||||||||||||
Medical condition: Severe Ocular Surface Disease (OSD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000294-33 | Sponsor Protocol Number: LX201-02 | Start Date*: 2007-07-27 | |||||||||||
Sponsor Name:Lux Biosciences, Inc. | |||||||||||||
Full Title: A MULTI-CENTER, PLACEBO-CONTROLLED, RANDOMIZED, PARALLEL-GROUP, DOSE-RANGING STUDY TO ASSESS THE EFFICACY AND SAFETY OF LX201 IMPLANTATION FOR THE PREVENTION OF CORNEAL ALLOGRAFT REJECTION EPISODES... | |||||||||||||
Medical condition: Patient after penetrating keratoplasty who have experienced one or more rejection episodes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005757-38 | Sponsor Protocol Number: OFTACAMPOS_08_01 | Start Date*: 2009-02-10 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: CORD BLOOD SERUM IN THE TREATMENT OF OCULAR SURFACE DISEASES (PILOT STUDY.) | |||||||||||||
Medical condition: severe ocular surface disorders and the enhancement of corneal wound healing | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005388-33 | Sponsor Protocol Number: GS101-P3-CG | Start Date*: 2009-02-03 |
Sponsor Name:Les Laboratoires CTRS | ||
Full Title: A MULTICENTRE DOUBLE-BLIND RANDOMIZED STUDY TO INVESTIGATE THE EFFICACY AND TOLERABILITY OF GS-101 EYE DROPS, AN ANTISENSE OLIGONUCLEOTIDE, VERSUS PLACEBO ON INHIBITION OF CORNEAL NEOVASCULARIZATIO... | ||
Medical condition: Patients with corneal neovascularization, a major risk factor of corneal graft rejection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) FR (Completed) | ||
Trial results: Removed from public view |
EudraCT Number: 2020-003408-15 | Sponsor Protocol Number: DMEC | Start Date*: 2021-06-14 |
Sponsor Name:Oslo University Hospital | ||
Full Title: A randomized clinical two-arm trial comparing inflammation and cystoid macular edema for the medication regimens postoperative topical NSAIDs and steroids to only postoperative topical steroids in ... | ||
Medical condition: Corneal disease/opacification treated with corneal endothelial transplantation (DSAEK or DMEK surgery), and the medical treatment is anti-inflammatory eye drops to treat (and prevent) intraocular i... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001543-19 | Sponsor Protocol Number: CSCTversion1.2 | Start Date*: Information not available in EudraCT |
Sponsor Name:Antwerp University Hospital (UZA) | ||
Full Title: Cultivated Limbal Stem Cell Transplantation for the Treatment of Limbal Stem Cell Deficiency. | ||
Medical condition: Patients suffering from Limbal Stem Cell Deficiency will be investigated during the course of this clinical trial. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004247-24 | Sponsor Protocol Number: CCRG13-003 | Start Date*: 2015-01-27 | ||||||||||||||||
Sponsor Name:Antwerp University Hospital (UZA) | ||||||||||||||||||
Full Title: Translational stem cell research in ophthalmology - regenerating the anterior cornea through standardized transplantation of limbal epithelial stem cells: a phase II multicenter trial | ||||||||||||||||||
Medical condition: Primary and secondary Limbal Stem Cell Deficiencies | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003215-63 | Sponsor Protocol Number: 69HCL19_0032 | Start Date*: 2020-03-10 | |||||||||||
Sponsor Name:Hospices Civils de Lyon - Direction de la Recherche Clinique et de l'Innovation | |||||||||||||
Full Title: Cultured Autologous Oral Mucosa Epithelial sheet for the Treatment of Bilateral Limbal Stem Cell Deficiency - FEMJA for « Feuillet Epithélial de Muqueuse Jugale Autologue » | |||||||||||||
Medical condition: Bilateral Limbal Stem Cell Deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000598-30 | Sponsor Protocol Number: CS001-EU01 | Start Date*: 2012-03-06 | |||||||||||
Sponsor Name:Cellseed France S.A.R.L. | |||||||||||||
Full Title: MULTICENTER STUDY OF CULTURED AUTOLOGOUS ORAL MUCOSAL EPITHELIAL CELL-SHEET (CAOMECS) TRANSPLANTATION TO PATIENTS WITH TOTAL LIMBAL STEM CELL DEFICIENCY | |||||||||||||
Medical condition: Limbal Stem Cell Deficiency of the Eye | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Ongoing) AT (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006792-42 | Sponsor Protocol Number: EAE120 | Start Date*: 2022-03-09 | |||||||||||
Sponsor Name:Hellenic Society of Hematology (EAE) | |||||||||||||
Full Title: A phase 1/2, dose and schedule evaluation study to investigate the safety and clinical activity of Belantamab Mafodotin administered in combination with Daratumumab, Lenalidomide and Dexamethasone ... | |||||||||||||
Medical condition: newly diagnosed multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005826-27 | Sponsor Protocol Number: EAE-2020/MM0107 | Start Date*: 2021-01-26 | |||||||||||
Sponsor Name:Hellenic Society of Hematology (EAE) | |||||||||||||
Full Title: A phase 1/2, dose and schedule evaluation study to investigate the safety and clinical activity of Belantamab Mafodotin administered in combination with Lenalidomide and Dexamethasone in patients w... | |||||||||||||
Medical condition: newly diagnosed multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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