- Trials with a EudraCT protocol (859)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
859 result(s) found for: Evolution.
Displaying page 1 of 43.
EudraCT Number: 2012-002834-36 | Sponsor Protocol Number: Retro-001 | Start Date*: 2012-09-13 |
Sponsor Name:UMCG | ||
Full Title: Evaluation of the effects of the addition of atropine during propofol/remifentanil induction of anesthesia on hemodynamics, microvascular blood flow and tissue oxygenenation in patients undergoing ... | ||
Medical condition: ophthalmic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000741-39 | Sponsor Protocol Number: 6996 | Start Date*: 2019-11-07 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: EFFECT OF AZITHROMYCIN ON THE PROPORTION OF FAILURES OF SEVERE PERIODONTITIS NON-SURGICAL TREATMENTS : A RANDOMIZED, DOUBLE-BLIND VERSUS PLACEBO STUDY | ||
Medical condition: Periodontology | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006474-23 | Sponsor Protocol Number: BTIIMD-01-EC/21/LIQUEN | Start Date*: 2022-03-16 |
Sponsor Name:BTI I MAS D S.L. | ||
Full Title: Randomized, treatment-controlled clinical trial Conventional efficacy of Plasma Rich in Factors of Growth (PRGF®) in the treatment of atrophic vulvar lichen sclerosus | ||
Medical condition: Vulvar Lichen Sclerosus et atrophicus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001220-35 | Sponsor Protocol Number: RC31-19-0045 | Start Date*: 2019-10-08 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: A randomized double-blinded pilot study of the efficacy and safety of dupilumab versus placebo in patients with Netherton syndrome | |||||||||||||
Medical condition: Netherton syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005681-37 | Sponsor Protocol Number: CL/BIO/15-005 | Start Date*: 2016-04-18 |
Sponsor Name:BIOIBERICA S.A. | ||
Full Title: Evaluation of the evolution of imaging markers of cartilage degradation in patients with knee osteoarthritis receiving DROGLICAN®: a Pilot Study | ||
Medical condition: Knee Osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005556-25 | Sponsor Protocol Number: OFT-ETAMSILATO-4.2.2 | Start Date*: 2015-05-11 |
Sponsor Name:Investigacion Independiente | ||
Full Title: Open extension study for patients with age related macula degeneration who participated in the Fase IV-II clinical trial randomized, simulatedcontrolled treatment to evaluate safety and efficacy o... | ||
Medical condition: Aged related macula degeneration (ARMD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005185-36 | Sponsor Protocol Number: FENOPRA-III-05-1 | Start Date*: 2006-02-10 |
Sponsor Name:Laboratoires SMB S.A. | ||
Full Title: AN OPEN-LABEL PHASE III, STUDY TO EVALUATE THE SAFETY OF THE COMBINATION (FENOFIBRATE / PRAVASTATIN 160-40 MG) DURING 24 WEEKS, IN HIGH VASCULAR RISK PATIENTS WITH COMBINED HYPERLIPIDEMIA | ||
Medical condition: High vascular risk patients with combined hyperlipidemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001812-36 | Sponsor Protocol Number: OFT-ETAMSILATO-4.2.3 | Start Date*: 2015-08-11 |
Sponsor Name:Dr. Pedro Cuevas Sanchez (Investigacion Independiente) | ||
Full Title: Extension study for the follow up of patients with age related macula degeneration who participated in the Fase IV-II clinical trial randomized, simulated controlled treatment to evaluate safety an... | ||
Medical condition: Aged related macula degeneration (ARMD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001892-34 | Sponsor Protocol Number: PI20208430041 | Start Date*: 2020-06-20 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: Treatment of COVID-19 by Nebulization of Inteferon Beta 1b added to lopinavir/ritonavir: Feasibility, Efficiency and Safety Study | ||
Medical condition: Infection SARS-Cov-2 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002830-19 | Sponsor Protocol Number: RC31-18-0269 | Start Date*: 2018-11-16 |
Sponsor Name: Toulouse University Hospital | ||
Full Title: A randomized, double blind placebo-controlled multicenter study of the efficacy and safety of dupilumab in patients with moderate to severe hand eczema refractory to highly potent topical corticost... | ||
Medical condition: Chronic hand eczema | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002669-13 | Sponsor Protocol Number: 87RI21_0052 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Limoges University Hospital | |||||||||||||
Full Title: The PENTO protocol in Medication-related osteonecrosis of the jaw (MRONJ): a single-center phase IIa trial | |||||||||||||
Medical condition: Medication-related osteonecrosis of the jaw (MRONJ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003202-27 | Sponsor Protocol Number: FAST-TOT401-19 | Start Date*: 2020-05-20 | |||||||||||
Sponsor Name:Laboratoire Innotech Internationnal | |||||||||||||
Full Title: Assessment of the eFficacy, the onset-of-Action and the Safety of Tot'héma ® in adults with moderate iron deficiency anaemia | |||||||||||||
Medical condition: Moderate iron deficiency anaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000633-39 | Sponsor Protocol Number: FEC-TH | Start Date*: 2012-05-21 |
Sponsor Name:Fundación para la Formación e Investigación Sanitaria | ||
Full Title: Extracorporeal photopheresis in liver transplantation. Clinical trial phase I/II safety and efficacy in patients with progressive withdrawal of immunosuppression. | ||
Medical condition: Liver transplantation more than 2 years of evolution to complications of immunosuppression. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004755-75 | Sponsor Protocol Number: MICROPREP | Start Date*: 2017-09-28 |
Sponsor Name:Clinique Juge | ||
Full Title: Intra articular injection of microfat and platelet-rich plasma in the treatment of knee osteoarthritis : a pilot study | ||
Medical condition: knee osteoarthritis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004756-38 | Sponsor Protocol Number: 2018-1201 | Start Date*: 2019-02-12 |
Sponsor Name:Institut de Cancérologie Lucien Neuwirth | ||
Full Title: Study of thromboelastography during tranexamic acid treatment in preventing bleeding in patients with haematological malignancies presenting severe thrombocytopenia (TTRAP-bleeding) | ||
Medical condition: Malignant hemopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001717-20 | Sponsor Protocol Number: COVIDIOL | Start Date*: 2020-04-20 | ||||||||||||||||
Sponsor Name:Fundación para la Investigación Biomédica de Córdoba | ||||||||||||||||||
Full Title: Prevention and treatment with Calcifediol of Coronavirus COVID-19-induced acute respiratory syndrome (SARS) | ||||||||||||||||||
Medical condition: Severe Acute Respiratory Syndrome in subjects with COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001197-42 | Sponsor Protocol Number: 2017-01 | Start Date*: 2017-05-15 |
Sponsor Name:ASSISATNCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: Evolution of the cardiac function(office) during the follow-up of the anticancer immunotherapy inhibiting PD-1 | ||
Medical condition: as melanoma, non-small cell lung cancers and kidney cancers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005259-20 | Sponsor Protocol Number: OFT-ETAMSILATO-4.2.1 | Start Date*: 2015-02-13 | |||||||||||
Sponsor Name:Investigacion Independiente | |||||||||||||
Full Title: FASE IV-II CLINICAL TRIAL, PROOF OF CONCEPT, RANDOMIZED, SIMULATED CONTROLLED TREATMENT, DOUBLE BLINDED AND UNICENTRIC WITH TWO PARALLEL GROUPS, TO EVALUATE SAFETY AND EFFICACY OF INTRAVITREAL ADMI... | |||||||||||||
Medical condition: Aged related macula degeneration (ARMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004480-31 | Sponsor Protocol Number: ALLOB-IF1 | Start Date*: 2014-05-27 | |||||||||||
Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
Full Title: A Pilot Phase IIa, Multicentre, Open, Proof-of-concept Study on the Safety and the Efficacy of Allogeneic Osteoblastic Cells (ALLOB®) implantation in Lumbar Spinal Fusion | |||||||||||||
Medical condition: Degenerative disc disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001481-23 | Sponsor Protocol Number: P160927J | Start Date*: 2017-09-12 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: MULTICENTER, RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED CLINICAL TRIAL WITH RILUZOLE IN SPINOCEREBELLAR ATAXIA TYPE 2 | |||||||||||||
Medical condition: SCA2 patients, both gender, at least 18 years of age | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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