- ICH GCP
- Registro de ensaios clínicos da UE
Últimos testes
EudraCT Number: 2004-004391-36 | Sponsor Protocol Number: AC-052-402 | Start Date: 2005-05-23 | ||||||
Sponsor Name: Actelion Pharmaceuticals Ltd. | ||||||||
Full Title: A multicenter, open-label, single-arm safety study to investigate the effects of chronic TRACLEER® treatment on testicular function in male patients with pulmonary arterial hypertension | ||||||||
Medical condition: Many endothelin receptor antagonists have profound effects on the histology and function of the testes in animals. These drugs have been shown to induce atrophy of the seminiferous tubules of the t... | ||||||||
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Population Age: Adults | Gender: Male | |||||||
Trial protocol: HU (Completed) CZ (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002096-16 | Sponsor Protocol Number: 01/04 | Start Date: 2005-05-23 | ||||||
Sponsor Name: Universitätskinderklinik Innsbruck | ||||||||
Full Title: Effect of plasma volume expansion with hydroxy-ethyl-starch (HES) 130/0.4 or crystalloids on interstitial fluid accumulation and blood pressure in newborn infants with arterial hypotension | ||||||||
Medical condition: Arterial hypotension | ||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |||||||
Trial protocol: AT (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002854-78 | Sponsor Protocol Number: BO17706 | Start Date: 2005-05-23 | |||||||||||
Sponsor Name: F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A randomised, double blind, placebo controlled, multicentre phase III trial to evaluate the efficacy and safety of adding bevacizumab to gemcitabine and erlotinib in patients with metastatic pancre... | |||||||||||||
Medical condition: Metastatic pancreatic cancer (adenocarcinoma) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) FI (Completed) GB (Completed) SE (Completed) CZ (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004124-12 | Sponsor Protocol Number: 55730 | Start Date: 2005-05-23 | |||||||||||
Sponsor Name: AZIENDA SANITARIA OSPEDALIERA O.I.R.M. - S. ANNA | |||||||||||||
Full Title: LACTOBACILLUS REUTERI REUTERIN AS A THERAPEUTIC AGENT IN INFANTILE COLIC A PROSPECTIVE STUDY. | |||||||||||||
Medical condition: TREATMENT OF INFANTILE COLIC IN BREASTFED INFANTS OF AGE BETWEEN 21 AND 90 DAYS | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001041-42 | Sponsor Protocol Number: VAC030 | Start Date: 2005-05-23 | ||||||
Sponsor Name: University of Oxford | ||||||||
Full Title: Assessment of protection against malaria by sporozoite challenge of healthy adults vaccinated with the virosomal vaccine PEV3A and FP9-MVA ME-TRAP | ||||||||
Medical condition: Plasmodium falciparum malaria | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-004384-29 | Sponsor Protocol Number: Levosepsis1 | Start Date: 2005-05-23 | ||||||
Sponsor Name: Dr GED DEMPSEY, University Hospital Aintree | ||||||||
Full Title: Double blind randomised controlled trial of Levosimendan versus Dopexamine in septic shock | ||||||||
Medical condition: Septic Shock | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003985-14 | Sponsor Protocol Number: CPR-EFC5816-EN-E01 | Start Date: 2005-05-23 | |||||||||||
Sponsor Name: Sanofi-Synthelabo Research | |||||||||||||
Full Title: A Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial Evaluating the Effect of Two Doses of a Vasopressin V2 Receptor Antagonist (SR121463B) on Serum Sodium in Patients with Dilutional ... | |||||||||||||
Medical condition: Dilutional hyponatremia excluding chronic syndrome of inappropriate antidiuretic hormone secretion (SIADH) or cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001507-19 | Sponsor Protocol Number: 04/5/025 | Start Date: 2005-05-22 | ||||||
Sponsor Name: National Children's Hospital & Trinity College Dublin | ||||||||
Full Title: Treatment with recombinant Growth Hormone in Children born Small for Gestational Age (SGA) without Catch-up Growth. | ||||||||
Medical condition: Short stature in children born small for gestational age without catch up growth | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: IE (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004512-23 | Sponsor Protocol Number: PKU-003 | Start Date: 2005-05-22 | |||||||||||
Sponsor Name: BioMarin Pharmaceutical Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Phenoptin in Subjects with Phenylketonuria Who Have Elevated Phenylalanine Levels | |||||||||||||
Medical condition: Phenylketonuria (PKU) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004924-11 | Sponsor Protocol Number: SHX0712 | Start Date: 2005-05-20 | ||||||
Sponsor Name: ALK-Abelló A/S | ||||||||
Full Title: A multicentre, randomised, double-blind, placebo-controlled parallel group clinical trial to investigate the efficacy and safety of specific sublingual immunotherapy with SLIT One birch in patients... | ||||||||
Medical condition: Desensibilisierung gegenüber Allergenen | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |