- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Nacre.
Displaying page 1 of 1.
EudraCT Number: 2018-003905-25 | Sponsor Protocol Number: HAC2018-001 | Start Date*: 2019-06-27 | |||||||||||
Sponsor Name:H.A.C. Pharma | |||||||||||||
Full Title: Evaluation of efficacy and tolerance of fludrocortisone (Flucortac) in the treatment of neurogenic orthostatic hypotension | |||||||||||||
Medical condition: Neurogenic Orthostatic Hypotension (NOH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000406-79 | Sponsor Protocol Number: 06-065 | Start Date*: 2007-07-06 |
Sponsor Name:CHU de Caen | ||
Full Title: Evolution clinique de la nucléolyse à l’éthanol sur la douleur, l’incapacité fonctionnelle et la qualité de vie de patients souffrant de sciatique ou de cruralgie par hernie discale. | ||
Medical condition: Adultes de plus de 18 ans présentant une sciatique ou une cruralgie résistante au traitement médical classique. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001631-55 | Sponsor Protocol Number: 07-026 | Start Date*: 2007-09-07 |
Sponsor Name:CHU de Caen | ||
Full Title: Evaluation des performances de l’échographie avec injection de produit de contraste (Sonovue®) dans la détection des métastases hépatiques synchrones ou métachrones d’un cancer colo-rectal. | ||
Medical condition: dans la détection des métastases hépatiques synchrones ou métachrones d’un cancer colo-rectal | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001842-42 | Sponsor Protocol Number: 07-009 | Start Date*: 2007-11-16 |
Sponsor Name:CHU de Caen | ||
Full Title: Fixation de prothèses par Tissucol dans la cure de prolapsus par voie vaginale | ||
Medical condition: women with pelvic organ prolapse | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002534-11 | Sponsor Protocol Number: 06-058 | Start Date*: 2008-05-19 | |||||||||||
Sponsor Name:CHU de Caen | |||||||||||||
Full Title: EFFICACITE D’UN TRAITEMENT PAR CINACALCET SUR LE METABOLISME OSSEUX CHEZ LES TRANSPLANTES RENAUX AVEC HYPERPARATHYROIDIE PERSISTANTE | |||||||||||||
Medical condition: LES TRANSPLANTES RENAUX AVEC HYPERPARATHYROIDIE PERSISTANTE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000080-85 | Sponsor Protocol Number: 17-245 | Start Date*: 2018-11-29 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Pilot study of the pharmacokinetic profile of paracetamol subcutaneously versus intravenously in patients receiving palliative care | |||||||||||||
Medical condition: Major patients in palliative care | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002531-30 | Sponsor Protocol Number: 20-079 | Start Date*: 2020-08-05 | |||||||||||
Sponsor Name:CHU CAEN Normandie | |||||||||||||
Full Title: ETUDE DE TOLERANCE DE LA N-ACETYLCYSTEINE POUR LA THROMBOLYSE A LA PHASE AIGUË DE L’INFARCTUS CEREBRAL | |||||||||||||
Medical condition: Patients atteints d’un infarctus cérébral non lacunaire bénéficiant d’un traitement par fibrinolyse intraveineuse (+/- thrombectomie mécanique). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015543-16 | Sponsor Protocol Number: 07-135 | Start Date*: 2010-07-27 | |||||||||||
Sponsor Name:CHU de Caen | |||||||||||||
Full Title: Evaluation diagnostique et pronostique de l’hypoxie dans les tumeurs cérébrales par le F-MISO en imagerie TEP et par des marqueurs biologiques en vue d'une meilleure orientation thérapeutique | |||||||||||||
Medical condition: brain tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002574-63 | Sponsor Protocol Number: 07-058 | Start Date*: 2007-07-27 | |||||||||||
Sponsor Name:CHU de Caen | |||||||||||||
Full Title: Essai randomisé de phase 2-3 testant l’association Pemetrexed-Cisplatine avec ou sans bevacizumab à 15 mg/kg, dans le mésothéliome malin de la plèvre (MPM). | |||||||||||||
Medical condition: pleural mesothelioma malignant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012592-10 | Sponsor Protocol Number: 09-057 | Start Date*: 2009-07-23 | |||||||||||
Sponsor Name:CHU Caen | |||||||||||||
Full Title: Méthode d’évaluation de l’aptitude à la conduite chez des patients souffrant de pathologies de l’éveil: cirrhose avec ou sans encéphalopathie (AutoSoP "foie"). | |||||||||||||
Medical condition: cirrhose | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005804-27 | Sponsor Protocol Number: 15-200 | Start Date*: 2016-06-04 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Essai randomisé, contrôlé, en double aveugle, de l'anakinra contre placebo, en adjonction à la corticothérapie dans l'artérite à cellules géantes. | |||||||||||||
Medical condition: Patients atteints d’artérite à cellules géantes (ou maladie de Horton) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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