- Trials with a EudraCT protocol (26,267)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
26,267 result(s) found for: NA.
Displaying page 57 of 1,314.
| EudraCT Number: 2004-004488-31 | Sponsor Protocol Number: S-02005 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Rikshospitalet University Hospital, University of Oslo | ||
| Full Title: Does cyclosporine A reduce the insulin secretion from the pancreas? | ||
| Medical condition: Kidney failure / dialysis patients / transplantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-002213-51 | Sponsor Protocol Number: 20080411 | Start Date*: 2008-07-04 |
| Sponsor Name:Puolustusvoimat, Sotilaslääketieteen keskus | ||
| Full Title: Typpihumalatesti sukeltajilla: Satunnaistettu nousu painekammiossa hengittämällä ilmaa, maskilla ilmaa tai maskilla happea. | ||
| Medical condition: Tutkittavat sukeltajat satunnaistetaan hengittämään ylipaineessa kosteaa ilmaa, kuivaa ilmaa ja kuivaa happea tarkoituksella löytää tapa, mikä vähentää sukeltajantaudin riskiä | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000403-33 | Sponsor Protocol Number: GEICAM/2004-04 | Start Date*: 2005-06-01 |
| Sponsor Name:GRUPO ESPAÑOL DE INVESTIGACIÓN EN CÁNCER DE MAMA (GEICAM) | ||
| Full Title: Randomized clinical trial to evaluate the predictive accuracy of a gene expression profile-based test to select patients for preoperative taxane/anthracycline chemotherapy for stage I-III breast ca... | ||
| Medical condition: Patients with histologically confirmed stage I-III invasive carcinoma of the breast for whom adjuvant chemotherapy is indicated. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003537-41 | Sponsor Protocol Number: VAN001/2005 | Start Date*: 2005-10-27 |
| Sponsor Name:TRICHOLOG GmbH | ||
| Full Title: Efficacy of the treatment with VANIQA 11,5% creme in patients suffering from hirsutism of the upper lip | ||
| Medical condition: Hirsutism of the upper lip in female patients suffering from increased hair growth in the face | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005471-15 | Sponsor Protocol Number: NZHD01 | Start Date*: 2006-03-27 |
| Sponsor Name:University of Heidelberg | ||
| Full Title: Real-time contrast-enhanced sonography of renal transplant recipients accurately predicts chronic allograft nephropathy | ||
| Medical condition: Chronic allograft nephropathy (CAN) represents the main cause of renal allograft loss after 1 yr of transplantation. The trial shall find a way for early diagnostics. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002554-29 | Sponsor Protocol Number: 2006-1 | Start Date*: 2006-10-09 |
| Sponsor Name:Hammel neurocenter | ||
| Full Title: Methylphenidat betydning for motorisk indlæring hos patienter med apopleksi | ||
| Medical condition: Patients less that 2 months after the first hemorrhagic or ischemic stroke. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004830-15 | Sponsor Protocol Number: S241-GB-02 | Start Date*: 2005-01-31 |
| Sponsor Name:Stiefel Laboratories Maidenhead Ltd (commonly known as Stiefel International R&D) | ||
| Full Title: Human Repeat Insult Patch Test with Challenge | ||
| Medical condition: Not Applicable (Healthy Volunteer Study) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-000333-36 | Sponsor Protocol Number: 17012006 | Start Date*: 2006-04-26 |
| Sponsor Name:Hull & East Yorkhire NHS Hospitals Trust | ||
| Full Title: A randomised comparison of 0.5% levobupivacaine with a lidocaine/epinephrine/ fentanyl mixture for epidural top up for emergency caesarean section after “low dose” epidural for labour | ||
| Medical condition: pregnant women, in labour requiring emergency caesarean section under epidural anaesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-001385-14 | Sponsor Protocol Number: IOBA-01-2004 | Start Date*: 2006-01-23 |
| Sponsor Name:IOBA. FACULTAD DE MEDICINA | ||
| Full Title: Evaluacion de la eficacia y seguridad de la inyección intravítrea de triamcinolona en el tratamiento del edema difuso del diabético | ||
| Medical condition: DIFFUSE DIABETIC MACULAR OEDEMA | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-001516-20 | Sponsor Protocol Number: AKF-374 | Start Date*: 2008-06-30 |
| Sponsor Name:Institut of Public Health | ||
| Full Title: Paroxetins effekt på tramadols metabolisme og farmakodynamik: et dosis respons studie | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-004686-15 | Sponsor Protocol Number: LUD 03-007 | Start Date*: 2005-08-04 |
| Sponsor Name:Ludwig Institute For Cancer Research | ||
| Full Title: Phase I/II study of immunization with multiple peptides mixed with the immunological adjuvant CpG 7909 in HLA-A2 patients with metastatic melanoma ... | ||
| Medical condition: HLA-A2 patients with metastatic melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-001587-31 | Sponsor Protocol Number: A001-2PX | Start Date*: 2005-06-07 |
| Sponsor Name:SantoSolve AS | ||
| Full Title: | ||
| Medical condition: Patients with fibromyalgia diagnosed according to ACR classification (1990) and with chronic pain at defined symmetrical body areas. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002882-19 | Sponsor Protocol Number: MCHT001 | Start Date*: 2004-12-10 |
| Sponsor Name:Mid Cheshire Hospitals NHS Trust | ||
| Full Title: A controlled trial into the benefit of topical perianal glyceryl trinitrate (GTN) as a sphincter relaxant, pre-insertion of ultrasound probe for trans rectal ultrasound (TRUS) guided biopsy of the ... | ||
| Medical condition: Prostate Cancer Diagnosis – Pain relief during biopsy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002947-94 | Sponsor Protocol Number: 260506 | Start Date*: 2006-07-25 |
| Sponsor Name:Minna Tallgren | ||
| Full Title: DEKSAMETASONIN VAIKUTUS RINTALEIKKAUKSEN JÄLKEISEN KIVUN HALLINTAAN - satunnaistettu, kakssoissokko, lumekontrolloitu tutkimus | ||
| Medical condition: rintakirurgiseen leikkaukseen liittyvän kivun hoito, yhdistettynä tavanomaiseen tässä tilanteessa käytettyyn kipulääkitykseen | ||
| Disease: | ||
| Population Age: Elderly | Gender: Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002732-22 | Sponsor Protocol Number: CL3-12911-019 | Start Date*: 2006-09-08 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: A double-blind, multicentric, multinational randomised study to assess the effects of two years administration of 2g per day of strontium ranelate versus alendronate 70mg per week in women with pos... | |||||||||||||
| Medical condition: Treatment of postmenopausal Osteoporosis to reduce the risk of hip and vertebral fractures | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004336-20 | Sponsor Protocol Number: LT1225-PII-04/08 | Start Date*: 2008-11-28 |
| Sponsor Name:Laboratoires Thea | ||
| Full Title: Azithromycin concentration into aqueous humor of patients undergoing cataract surgery, after 3 days of treatment by AZYTER ® Open randomised monocentre study with 2 groups of 15 patients | ||
| Medical condition: Patient concerned by this trial are patients who will undergo a cataract surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023662-47 | Sponsor Protocol Number: Rifa-2 | Start Date*: 2010-12-13 |
| Sponsor Name:Oulu University Hospital, Department of Internal Medicine | ||
| Full Title: PXR-aktivaation vaikutukset sokeri-, kolesteroli- ja hormonitasapainoon | ||
| Medical condition: Terveitä vapaaehtoisia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-018486-37 | Sponsor Protocol Number: dexa2010 | Start Date*: 2010-05-21 |
| Sponsor Name:Kris-och Traumacentrum | ||
| Full Title: Treatment of exacerbations of post-traumatic stress disorder by short-term dexamethasone, a pilot study. | ||
| Medical condition: Posttraumatic stress syndrome F431 | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001543-36 | Sponsor Protocol Number: 091257-2005 | Start Date*: 2006-05-15 |
| Sponsor Name:NHS Lothian | ||
| Full Title: The effects of lipoic acid on glycaemic control in type 2 diabetes. | ||
| Medical condition: Type 2 diabetes mellitus. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001841-32 | Sponsor Protocol Number: SVS20-ESP-03-02 | Start Date*: 2006-06-23 |
| Sponsor Name:TRBChemedica | ||
| Full Title: Eficacia y Seguridad de SVS20 en pacientes con síndrome de ojo seco moderado bilateral: Estudio Piloto de 3 meses, fase II, aleatorio de pares correspondientes, controlado y enmascarado para el eva... | ||
| Medical condition: Ojo Seco | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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