- Trials with a EudraCT protocol (200)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
200 result(s) found for: Collagen disease.
Displaying page 1 of 10.
EudraCT Number: 2013-001221-13 | Sponsor Protocol Number: 2639063 | Start Date*: 2013-10-10 | |||||||||||
Sponsor Name:Akershus university hospital | |||||||||||||
Full Title: Dupytren’s disease study A randomized controlled trial comparing clostridium histolyticum with needle aponeurotomy. | |||||||||||||
Medical condition: Dupytren’s disease, primary MCP joint contractures of the third, forth and fifth finger of the hand. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000908-17 | Sponsor Protocol Number: Siena Eye Cross Linking 2004 | Start Date*: 2007-01-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: Medical therapy of keratoconus with Riboflavin/Ultraviolet-A collagen Cross-Linking and investigation of the corneal stromal and Keratocytes modifications apoptosis and stromal repopulation with ... | |||||||||||||
Medical condition: Patients affected by keratoconus worsening | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021664-16 | Sponsor Protocol Number: SVUH | Start Date*: 2010-11-04 | |||||||||||
Sponsor Name:Solvotrin Innovations Ltd | |||||||||||||
Full Title: The role of doxycycline in the management of diastolic dysfunction | |||||||||||||
Medical condition: Diastolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2013-000639-29 | Sponsor Protocol Number: ABCSG_P00 | Start Date*: 2013-03-27 | ||||||||||||||||
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||||||||||||||||||
Full Title: A prospective, open, randomized, academic phase II, two-arm trial evaluating the effect of fibrin-coated collagen (TachoSil®) on postoperative pancreatic leakage and fistula formation from the panc... | ||||||||||||||||||
Medical condition: pancreatic surgery - evaluation of the effect of fibrin-coated collagen | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004882-26 | Sponsor Protocol Number: ND-L02-s0201-002 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:Nitto Denko Corporation | |||||||||||||
Full Title: A Phase 1b/2, Open Label, Randomized, Repeat Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, Biological Activity and Pharmacokinetics of ND L02 s0201 Injection, a Vitamin A-couple... | |||||||||||||
Medical condition: Moderate to extensive progressive hepatic fibrosis (METAVIR F3-4) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004347-10 | Sponsor Protocol Number: 20080009 | Start Date*: 2009-06-17 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Prospective, Phase IV, Open-Label, Multi-Center Study Evaluating Changes in Bone Marrow Morphology in Adult Subjects Receiving Romiplostim for the Treatment of Thrombocytopenia Associated with Im... | |||||||||||||
Medical condition: Thrombocytopenia associated with ITP | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) DE (Completed) PL (Completed) BE (Completed) ES (Completed) HU (Completed) SE (Completed) EE (Completed) IT (Completed) LT (Completed) SI (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005999-13 | Sponsor Protocol Number: D8180C00034 | Start Date*: 2008-02-21 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II, Randomised, Open-label, Pilot Study to Evaluate the Safety and the Effects on Bone Resorption of AZD0530 in Patients with Prostate Cancer or Breast Cancer with Metastatic Bone Disease ... | ||
Medical condition: Prostate Cancer or Breast Cancer with Metastatic Bone Disease Cáncer de próstata o de mama con metástasis óseas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) GB (Completed) SE (Completed) PT (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003216-37 | Sponsor Protocol Number: n.a. | Start Date*: 2015-02-12 |
Sponsor Name: | ||
Full Title: Efficacy of Verapamil/ Verapamil-Kenacort injection versus Kenacort injection in Scar Treatment | ||
Medical condition: Hypertrophic and keloid scars are pathological scars as a result of dermal injury and exhibit exuberant, indefinite growth of collagen during wound healing. Hypertrophic and keloid scars often caus... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-006023-33 | Sponsor Protocol Number: SIMFIB | Start Date*: 2021-10-26 | ||||||||||||||||
Sponsor Name:Institut d’Investigacions Biomèdiques August Pi i Sunyer | ||||||||||||||||||
Full Title: Efficacy of simvastatin reducing liver fibrosis in patients with advanced fibrosis due to alcohol: a randomized, double-blind, placebo-controlled clinical trial. | ||||||||||||||||||
Medical condition: reduction of liver fibrosis in patients with advanced fibrosis due to alcohol | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001929-40 | Sponsor Protocol Number: AZT_DSTB_BB | Start Date*: 2017-11-21 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: A prospective, randomized pilot study of the immunomodulatory effects of azithromycin in adults with pulmonary tuberculosis | |||||||||||||
Medical condition: Pulmonary tuberculosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003670-32 | Sponsor Protocol Number: REFLECT | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Medical Center - University of Freiburg | |||||||||||||
Full Title: A dual-center prospective phase I/II trial to establish safety, tolerability and to obtain first data on efficacy of losartan in children with recessive dystrophic epidermolysis bullosa (RDEB) | |||||||||||||
Medical condition: Recessive dystrophic epidermolysis bullosa (RDEB) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004592-74 | Sponsor Protocol Number: HOLOGENE7(HTA-HG7-01) | Start Date*: 2016-06-01 |
Sponsor Name:Holostem Terapie Avanzate s.r.l. | ||
Full Title: PROSPECTIVE, OPEN LABEL, UNCONTROLLED CLINICAL TRIAL TO ASSESS THE SAFETY AND EFFICACY OF AUTOLOGOUS CULTURED EPIDERMAL GRAFTS CONTAINING EPIDERMAL STEM CELLS GENETICALLY MODIFIED WITH A GAMMA-RETR... | ||
Medical condition: RDEB is characterized by generalized skin blistering, erosions, crusts, atrophic scarring, onychodystrophy and loss of nails, mutilating pseudosyndactyly of hands and feet, as well as oral cavity l... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003890-91 | Sponsor Protocol Number: BIOOPA | Start Date*: 2020-09-29 | |||||||||||
Sponsor Name:Medical University of Warsaw | |||||||||||||
Full Title: The development of innovative advanced therapy medicinal product (biological dressing of the human race) in the treatment of Epidermolysis Bullosa (EB) and other chronic wounds. | |||||||||||||
Medical condition: BIOOPA dressing will be used in the treatment of wounds in the course of Epidermolysis Bullosa, chronic venous leg ulceration and thermal injury (second degree burn). | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000934-31 | Sponsor Protocol Number: INN-TOP-005 | Start Date*: 2015-07-10 | |||||||||||
Sponsor Name:Innocoll Pharmaceuticals Limited | |||||||||||||
Full Title: A Phase 3 Randomized, Placebo-Controlled, Blinded Study to Investigate the Safety and Efficacy of a Topical Gentamicin-Collagen Sponge in Combination with Systemic Antibiotic Therapy in Diabetic Pa... | |||||||||||||
Medical condition: Diabetic Patients with an Infected Foot Ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) AT (Completed) BE (Completed) ES (Completed) SK (Completed) NL (Completed) GB (Completed) PL (Completed) HU (Completed) DK (Completed) LV (Completed) LT (Completed) EE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002015-38 | Sponsor Protocol Number: ISD002-P144-07 | Start Date*: 2007-08-23 | |||||||||||
Sponsor Name:ISDIN | |||||||||||||
Full Title: "ENSAYO CLÍNICO MULTICÉNTRICO, FASE II, ALEATORIZADO, DOBLE CIEGO, CONTROLADO INTRAINDIVIDUALMENTE CON PLACEBO, PARA EVALUAR LA EFICACIA Y SEGURIDAD DE P144 EN EL TRATAMIENTO TÓPICO DE LA FIBROSIS ... | |||||||||||||
Medical condition: "FIBROSIS CUTÁNEA DE PACIENTES CON ESCLEROSIS SISTÉMICA" "SKIN FIBROSIS IN PATIENTS WITH SYSTEMIC SCLEROSIS" | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) HU (Completed) GB (Completed) DE (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004806-17 | Sponsor Protocol Number: PQ-313-002 | Start Date*: 2018-05-18 | |||||||||||
Sponsor Name:Wings Therapeutics Inc. | |||||||||||||
Full Title: A first in human, double-blind, randomized, intra-subject placebo-controlled, multiple dose study of QR-313 evaluating safety, proof of mechanism, preliminary efficacy and systemic exposure in subj... | |||||||||||||
Medical condition: Recessive Dystrophic Epidermolysis Bullosa (RDEB) due to mutation(s) in exon 73 of the COL7A1 gene | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Prematurely Ended) DE (Prematurely Ended) CZ (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004325-10 | Sponsor Protocol Number: ME/2005/2018 | Start Date*: 2005-08-16 |
Sponsor Name:United Bristol Healthcare Trust | ||
Full Title: Evaluate Whether A Short Course Of Once Weekly Risedronate Prevents Bone Loss Following High-Dose Steroid Therapy For An Acute Exacerbation Of Inflammatory Bowel Disease. | ||
Medical condition: We aim to determine whether Risedronate is effective at preventing acute bone loss associated with a short course of corticosteroid (CS) therapy to treat exacerbations of inflammatory bowel disease... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001411-71 | Sponsor Protocol Number: R475-OA-1815 | Start Date*: 2018-12-03 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: Study to Evaluate Synovial Fluid in the Phase 3 Fasinumab Program for Osteoarthritis of the Knee and Hip | |||||||||||||
Medical condition: Pain due to osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000674-30 | Sponsor Protocol Number: 2013-000674-30 | Start Date*: 2013-07-24 |
Sponsor Name:AOU SAN LUIGI GONZAGA - SCDU ONCOLOGIA MEDICA | ||
Full Title: Multicenter clinical trial, randomized phase II "window of opportunity" which aims to test the biological activity of abiraterone acetate administered as neoadjuvant therapy in patients with prosta... | ||
Medical condition: PROSTATE CANCER PATIENTS WITH HIGH RISK | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000605-72 | Sponsor Protocol Number: CB+MSCforEB | Start Date*: 2014-02-06 |
Sponsor Name:Universitair Medisch Centrum Utrecht | ||
Full Title: Unrelated cord blood transplantation after reduced toxicity conditioning with mesenchymal stromal cell co-infusion in patients with severe epidermolysis bullosa | ||
Medical condition: The source population consists of patients referred to or within the UMC Groningen because they have diagnosed clinically and genetically severe generalized RDEB. | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
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