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EudraCT Number: 2019-000845-12 Sponsor Protocol Number: 070219 Start Date:
Sponsor Name: Canisius Wilhelmina Ziekenhuis
Full Title: The effectiveness of vitamin D suppletion on improving symptoms of fatigue in children between 12 and 18 years old
Medical condition: Fatigue
Disease: Version SOC Term Classification Code Term Level
Population Age: Adolescents, Under 18 Gender: Male, Female
Trial protocol: NL (Ongoing)
Trial results: (No results available)

EudraCT Number: 2008-003362-26 Sponsor Protocol Number: H552000-0809 Start Date:
Sponsor Name: Almirall Hermal GmbH
Full Title: A phase IIa single-center, randomized, controlled, observer-blind study to investigate the antimicrobial efficacy of topical formulations containing octenidine and prednicarbate in an"expanded flor...
Medical condition: Healthy volunteer trial to investigate whether topical formulations containing Octenidine and Octenidine plus Prednicarbate exert an in vivo antibacterial action on skin surface bacteria multiplied...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results
EudraCT Number: 2005-000051-15 Sponsor Protocol Number: A4061008 Start Date:
Sponsor Name: Pfizer Pharma GmbH
Full Title: Continuing Access to the Tyrosine Kinase Inhibitor of VEGFR-2, AG-013736 (A406) for Patients Previously Receiving AG-013736 in Clinical Trials
Medical condition: Patients who have been treated in previous AG-013736 oncology studies
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) CZ (Completed) IT (Completed) HU (Ongoing)
Trial results: (No results available)

EudraCT Number: 2010-018940-15 Sponsor Protocol Number: FLDX-001 Start Date:
Sponsor Name: SALUS Haus GmbH & Co. KG
Full Title: A Phase IV, multi-centre, randomized, open label study to investigate the efficacy and safety of Floradix® mit Eisen and ferro sanol® duodenal mite 50 mg in pregnant women with diagnosed iron defic...
Medical condition: Pregnant women with diagnosed iron deficiency
Disease: Version SOC Term Classification Code Term Level
12.1 10022976 Iron deficiency anemia secondary to inadequate dietary iron intake LLT
Population Age: Adults Gender: Female
Trial protocol: DE (Completed)
Trial results: (No results available)
EudraCT Number: 2020-003010-12 Sponsor Protocol Number: APHP180600 Start Date:
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title: «Efficacy of Fluticasone Propionate associated with Salmeterol using inhalation chamber versus placebo to improve the respiratory function in children over six years of age who underwent allogeneic...
Medical condition: Bronchiolitis Obliterative Syndrome after hematopoietic stem cell transplantation (HSCT). .
Disease: Version SOC Term Classification Code Term Level
Population Age: Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: FR (Ongoing)
Trial results: (No results available)

EudraCT Number: 2018-004494-27 Sponsor Protocol Number: 5020DERM-2018 Start Date:
Sponsor Name: Landeskrankenhaus Salzburg
Full Title: pilotstudy- efficacy of infectoscab 5% creme in patients with scabies
Medical condition: Scabies
Disease: Version SOC Term Classification Code Term Level
20.1 10021881 - Infections and infestations 10039511 Scabies LLT
20.0 10021881 - Infections and infestations 10063409 Acarodermatitis PT
Population Age: Children, Adolescents, Under 18, Adults, Elderly Gender: Male, Female
Trial protocol: AT (Ongoing)
Trial results: (No results available)
EudraCT Number: 2020-004933-19 Sponsor Protocol Number: DROPROP1 Start Date:
Sponsor Name: Region Västra Götaland, Sahlgrenska Universitetssjukhuset
Full Title: A Randomized Intervention, Multi-Center Study to Determine the Role of Dexamethasone eye drops against proliferative retinopathy of prematurity
Medical condition: Retinopathy of Prematurity
Disease: Version SOC Term Classification Code Term Level
20.1 100000004853 10036858 Proliferative retinopathy LLT
Population Age: Preterm newborn infants, Infants and toddlers, Under 18 Gender: Male, Female
Trial protocol: SE (Ongoing)
Trial results: (No results available)

EudraCT Number: 2020-004617-12 Sponsor Protocol Number: INTEGRATE_IIb Start Date:
Sponsor Name: Australasian Gastro-Intestinal Trials Group (AGITG)
Full Title: INTEGRATE IIb - A Randomised Phase III Open Label Study of regorafenib + nivolumab vs standard chemotherapy in Refractory Advanced Gastro-Oesophageal Cancer (AGOC)
Medical condition: refractory, advanced gastro-oesophageal cancer
Disease: Version SOC Term Classification Code Term Level
20.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10062878 Gastrooesophageal cancer PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: AT (Ongoing)
Trial results: (No results available)
EudraCT Number: 2016-002324-92 Sponsor Protocol Number: P150904 Start Date:
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title: Efficiency of Levamisole for Maintaining Remission After the First Flare of Steroid Sensitive Nephrotic Syndrome in Children (NEPHROVIR3)
Medical condition: Sensitive nephrotic syndrome in children
Disease: Version SOC Term Classification Code Term Level
19.1 10038359 - Renal and urinary disorders 10029164 Nephrotic syndrome PT
Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
Trial protocol: FR (Completed)
Trial results: (No results available)

EudraCT Number: 2004-000195-13 Sponsor Protocol Number: V59P5 Start Date:
Sponsor Name: Novartis Vaccines and Diagnostics
Full Title: A Phase II, Randomized, Open label, Controlled, Multicenter Study to Evaluate the Safety, Immunogenicity and Induction of Immunological Memory after Two or Three Doses of Novartis Meningococcal ACW...
Medical condition: Prevention of invasive disease caused by Neisseria Meningitidis serogroup A, C, W-135 and Y
Disease: Version SOC Term Classification Code Term Level
Population Age: Infants and toddlers, Under 18 Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: (No results available)
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