- Trials with a EudraCT protocol (726)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
726 result(s) found for: Abnormality.
Displaying page 1 of 37.
EudraCT Number: 2014-003817-28 | Sponsor Protocol Number: 2014-003817-28 | Start Date*: 2015-09-21 |
Sponsor Name:Region Östergötland | ||
Full Title: Does bisfosfonat preserve the bone volume in transplanted bone in the jaw? | ||
Medical condition: Jaw abnormality | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003732-22 | Sponsor Protocol Number: M7-1, Version 1, 03/08/05 | Start Date*: 2005-10-03 |
Sponsor Name:Kings College London | ||
Full Title: Pilot study of 5 Azacitidine in the treatment of MDS/AML with high risk (chromosome 7 and/or complex cytogenetic abnormality) | ||
Medical condition: myelodysplastic syndromes/relapsed Acute myeloid leukaemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-004981-16 | Sponsor Protocol Number: 1991-201-008 | Start Date*: 2022-06-17 | |||||||||||
Sponsor Name:Editas Medicine, Inc. | |||||||||||||
Full Title: Open-Label, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Efficacy of EDIT-101 in Adult and Pediatric Participants with Leber Congenital Amaurosis Type 10 (LCA10), with Cen... | |||||||||||||
Medical condition: Leber Congenital Amaurosis Type 10 (LCA10), with Centrosomal Protein 290 (CEP290)-Related Retinal Degeneration Caused by a Compound Heterozygous or Homozygous Mutation Involving c.2991+1655A>G in I... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002437-39 | Sponsor Protocol Number: SPI-103 | Start Date*: 2004-12-21 |
Sponsor Name:Daiichi Asubio Pharmaceuticals Inc. | ||
Full Title: A Phase IIb Randomized, Double-Blind, Placebo-Controlled, Group-Sequential, Multicenter, Dose Finding Study of the Safety and Efficacy of SUN N4057 (Piclozotan)Administered for 72 Hours by Continuo... | ||
Medical condition: Treatment of acute stroke. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) ES (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006937-28 | Sponsor Protocol Number: OPHT-040908 | Start Date*: 2009-03-30 | ||||||||||||||||
Sponsor Name:Universitätsklinik für Klinische Pharmakologie | ||||||||||||||||||
Full Title: Effect of Rosuvastatin on endothelial function in patients with diabetes and glaucoma | ||||||||||||||||||
Medical condition: volunteers with Diabetes type I or II and volunteers with Glaucoma are included Glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004852-52 | Sponsor Protocol Number: OPHT-141117 | Start Date*: 2018-04-17 |
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | ||
Full Title: The effect of Tetrahydrocannabinol on ocular hemodynamics in healthy subjects | ||
Medical condition: The study will be carried out in healthy subjects. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-005101-29 | Sponsor Protocol Number: KCH-MDS-04-1.0 | Start Date*: 2005-02-24 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust [...] | |||||||||||||
Full Title: THE EFFICACY AND SAFETY OF LENALIDOMIDE (Revlimid®) MONOTHERAPY IN RED BLOOD CELL TRANSFUSION DEPENDENT SUBJECTS WITH MYELODYSPLASTIC SYNDROME ASSOCIATED WITH A DEL (5q) CYTOGENETIC ABNORMALITY | |||||||||||||
Medical condition: Myelodysplastic Syndrome (MDS) associated with a Del (5q) cytogenetic abnormality | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002273-41 | Sponsor Protocol Number: OPHT-110106 | Start Date*: 2006-06-12 |
Sponsor Name:Medical University of Vienna; Clinical Pharmacology | ||
Full Title: Effect of antioxidants on ocular blood flow, endothelial function, and cytokine levels in LPS induced inflammatory model in humans. | ||
Medical condition: only healthy volunteers are involved | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000734-13 | Sponsor Protocol Number: V 1.0 | Start Date*: 2006-07-31 |
Sponsor Name:Department of Clinical Pharmacology | ||
Full Title: Effect of L-NMMA on retinal and choroidal blood flow in smokers compared to non-smokers. | ||
Medical condition: 24 healthy male and female volunteers, age 18-35 yrs., smokers (at least 10 cigarettes/day since 2 years) 24 healthy male and female volunteers, age 18-35 yrs., nonsmokers (since at least 2 years). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-005896-14 | Sponsor Protocol Number: Version 1.0 | Start Date*: 2006-02-20 |
Sponsor Name:Department of Clinical Pharmacology | ||
Full Title: Role of endothelin- and nitric oxide-system in the regulation of optic nerve head blood flow during changes in ocular perfusion pressure | ||
Medical condition: 18 healthy male volunteers Age 18-35 yrs., nonsmokers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-010138-22 | Sponsor Protocol Number: OPHT-101108 | Start Date*: 2009-04-02 |
Sponsor Name:Universitätsklinik für Klinische Pharmakologie | ||
Full Title: Effect of antioxidants on oxygen induced vasoconstriction in LPS induced inflammatory model in humans | ||
Medical condition: Healthy volunteers are included | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006981-40 | Sponsor Protocol Number: hypertension2006-006981-40 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust jointly with University of Cambridge | |||||||||||||
Full Title: Does the underlying haemodynamic abnormality determine response to antihypertensive therapy in patients with hypertension? | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) EE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014301-14 | Sponsor Protocol Number: 2009-014301-14 | Start Date*: 2009-07-15 | ||||||||||||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||||||||||||
Full Title: Farmacologic prevention with Varenicline in heavy smokers undergoing early detection lung cancer screening | ||||||||||||||||||||||||||||
Medical condition: Heavy smokers with higher risk in developing lung cancer and smoke related diseases | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001310-34 | Sponsor Protocol Number: OXY-COUP-PROT1.4 | Start Date*: 2011-08-11 |
Sponsor Name:Med. Univ. Wien, Univ. Klinik für Innere Med. III | ||
Full Title: Female Sexual Dysfunction in the Peri and Postmenopause: Effect of intranasal Oxytocin administration on sexual function and activity | ||
Medical condition: Sexual behaviour with reduced intercourse frequency due to female sexual function disorders | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004205-26 | Sponsor Protocol Number: Assente | Start Date*: 2006-07-14 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO IRCCS | |||||||||||||
Full Title: A Randomised controlled tiral to evaluate the efficacy of low molecular-weight heparin on pregnancy outcome of women with previus pregnancy complication | |||||||||||||
Medical condition: To asses wether the treatment with LMWH in Women with previus pregnancy complications and no evidence of anatomical, endocrine, Cromosmal or immunological abnormality result in a 40 reduction in t... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001498-13 | Sponsor Protocol Number: 24/2006/O/Sper | Start Date*: 2006-09-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Effetti della iniezione endovitreale di Avastin per il trattamento delle maculopatie essudative | |||||||||||||
Medical condition: exudative maculopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003901-10 | Sponsor Protocol Number: 250317BS | Start Date*: 2006-12-06 |
Sponsor Name:Neosil Inc. | ||
Full Title: A randomized, placebo controlled, double-blind study to evaluate the efficacy of topical formulations in male subjects with androgenetic alopecia | ||
Medical condition: The study will be performed in male subjects with Norwood/Hamilton grades III - IV, androgenetic alopecia. | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002710-23 | Sponsor Protocol Number: P140203 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000547-34 | Sponsor Protocol Number: QoL-ESC RevMDS | Start Date*: 2008-06-09 | |||||||||||
Sponsor Name:ASSOCIAZIONE QOL-ONE | |||||||||||||
Full Title: Lenalidomide for Myelodysplastic Syndromes: Efficacy, Safety, Cardiac Changes, and Quality of Life (QoL-ESC RevMDS) | |||||||||||||
Medical condition: Low or Intermediate-1 IPSS risk MDS with del(5q)as a single or combined cytogenetic abnormality and with anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020157-13 | Sponsor Protocol Number: HZA111789 | Start Date*: 2010-09-20 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: An open-label, non-randomized, pharmacokinetic and safety study of repeat doses of fluticasone furoate and GW642444M combination in healthy subjects and in subjects with mild, moderate or severe he... | |||||||||||||
Medical condition: healthy subjects and in subjects with mild, moderate or severe hepatic impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
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