- Trials with a EudraCT protocol (2,318)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,318 result(s) found for: Objective tests.
Displaying page 1 of 116.
EudraCT Number: 2014-001801-42 | Sponsor Protocol Number: EPU-P76 | Start Date*: 2014-11-25 |
Sponsor Name:Maastricht University | ||
Full Title: Sensitivity of driving-related psychometric tests to the effects of two widely prescribed benzodiazepines: diazepam and oxazepam | ||
Medical condition: None | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002722-23 | Sponsor Protocol Number: NL44755.044.13 | Start Date*: 2013-07-09 |
Sponsor Name:Medisch Spectrum Twente | ||
Full Title: The protective effect of a single dose inhaled steroid with different body postures against exercise induced bronchoconstriction | ||
Medical condition: Exercise Induced Bronchoconstriction | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002964-22 | Sponsor Protocol Number: AGO/2013/009 | Start Date*: 2013-12-10 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Influence of aromatase inhibitors on insulin sensitivity, liver and hart function in obese men | ||
Medical condition: Influence of aromatase inhibitors on insulin sensitivity, liver and hart function in obese men | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023980-17 | Sponsor Protocol Number: Metformin 3.0 | Start Date*: 2011-08-24 |
Sponsor Name:St. Antonius Hospital | ||
Full Title: An efficacy, safety and pharmacokinetic study on the short-term and long-term use of METFORMIN in obese children and adolescents | ||
Medical condition: obese children and adolescents of Caucasian descent with insulin resistance in the age of ≥ 10 and ≤ 16 years at study entry. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003958-25 | Sponsor Protocol Number: PI18/01097 | Start Date*: 2019-10-25 |
Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla | ||
Full Title: Screening for cancer with PET / CT in patients with unprovoked venous thromboembolic disease with a high risk of developing cancer. Open randomized clinical trial. | ||
Medical condition: Venous thromboembolic disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000682-30 | Sponsor Protocol Number: 01-09.02.15. | Start Date*: 2015-04-27 | |||||||||||
Sponsor Name:Tartu University Hospital | |||||||||||||
Full Title: Botulinum neurotoxin type A treatment for sialorrhea in central nervous system diseases | |||||||||||||
Medical condition: Hypersalivation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005411-16 | Sponsor Protocol Number: NASH-EX-1114 | Start Date*: 2015-06-30 |
Sponsor Name:Exalenz Bioscience Ltd. | ||
Full Title: Clinical Study of the BreathID® System to train the algorithm for the 13C-Octanoate Breath Test with or without the 13C-Methacetin Breath Test (OBT and MBT respectively) for correlation with histol... | ||
Medical condition: Patients with Non-Alcoholic Fatty Liver Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Ongoing) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004297-34 | Sponsor Protocol Number: 236252 | Start Date*: 2018-03-31 | |||||||||||
Sponsor Name:Aston University | |||||||||||||
Full Title: A placebo controlled double blind randomised controlled proof of concept study of zolpidem for the treatment of motor and cognitive deficits in late-stage Parkinson’s | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005916-26 | Sponsor Protocol Number: S241-GB-09 | Start Date*: 2006-02-01 |
Sponsor Name:Stiefel Laboratories Maidenhead Ltd | ||
Full Title: A phase I, single-blind, CPO solution human repeat insult patch test in healthy subjects. | ||
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: 2013-002769-20 | Sponsor Protocol Number: NL45149.044.13 | Start Date*: 2013-09-04 |
Sponsor Name:Medisch Spectrum Twente | ||
Full Title: The protective effect of a single dose salbutamol against exercise induced inspiratory airflow obstruction in asthmatic children. | ||
Medical condition: Exercise induced bronchoconstriction | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003543-67 | Sponsor Protocol Number: 2007-285-31-3 | Start Date*: 2007-10-30 |
Sponsor Name:Karolinska Universitetssjukhuset | ||
Full Title: Assessment of bronchial hyperresponsiveness in children - inhalation of Mannitol compared to eucapnic voluntary hyperventilation and methacholine provocation | ||
Medical condition: Three different methods to assess airway hyperresponsiveness in children with allergic asthma will be compared. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001512-38 | Sponsor Protocol Number: EPU-P87 | Start Date*: 2016-10-10 |
Sponsor Name:Maastricht University | ||
Full Title: Investigation of psychomotor performance to evaluate clinical impairment and pharmacokinetic aspects of methadone and buprenorphine: a double-blind placebo-controlled randomized trial | ||
Medical condition: None | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002480-26 | Sponsor Protocol Number: PRO_2013-02 | Start Date*: 2014-10-27 | |||||||||||
Sponsor Name:BIOSE | |||||||||||||
Full Title: Study of the efficacy and safety of treatment with total freeze-dried culture of Lcr Regenerans® administered intravaginally in the prevention of recurrent vulvovaginal candidiasis. International, ... | |||||||||||||
Medical condition: Recurrent vulvo-vaginal candidiasis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004612-22 | Sponsor Protocol Number: FP-01.1_CS_04 | Start Date*: 2013-12-24 | |||||||||||
Sponsor Name:Immune Targeting Systems Ltd | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study to assess the safety, tolerability, efficacy and immunogenicity of an influenza A vaccine (Vaccine FP-01.1) in healthy volunteers following viru... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000091-14 | Sponsor Protocol Number: FFR102123 | Start Date*: 2004-09-17 |
Sponsor Name:GlaxoSmithKline, S.A | ||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Multicentre, Long-Term Study to Evaluate the Safety of Once-Daily, Intranasal Administration of GW685698X Aqueous Nasal Spray 100mcg ... | ||
Medical condition: Perennial allergic rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) SE (Completed) LV (Completed) LT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001528-37 | Sponsor Protocol Number: Cholzuur | Start Date*: 2020-04-09 |
Sponsor Name:Cbusinez | ||
Full Title: Long-term safety study of personalized magistral prepared cholic acid capsules in patients with bile acid synthesis defects | ||
Medical condition: Patients with phenotypically mild Zellweger Spectrum Disorder (ZSD) or a Single Enzyme Defect (SED) in bile acid synthesis. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001427-40 | Sponsor Protocol Number: ION-682884-CS13 | Start Date*: 2022-06-07 | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open-Label, Extension Study to Assess the Long-Term Safety and Efficacy of ION-682884 in Patients with Hereditary Transthyretin-Mediated Amyloid Polyneuropathy | |||||||||||||
Medical condition: Hereditary Transthyretin-Mediated Amyloid Polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Trial now transitioned) ES (Ongoing) SE (Trial now transitioned) IT (Trial now transitioned) FR (Trial now transitioned) CY (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003165-34 | Sponsor Protocol Number: IRST100.11 | Start Date*: 2013-12-03 | |||||||||||
Sponsor Name:IRCCS-IRST of Meldola | |||||||||||||
Full Title: Peptide Receptor Radionuclide Therapy (PRRT) with Radiolabelled Somatostatin Analogue 177Lu-DOTATATE in advanced gastro-entero-pancreatic Neuroendocrine Tumors, FDG-PET negative patients: a prospe... | |||||||||||||
Medical condition: Advanced gastro-entero-pancreatic Neuroendocrine Tumors, FDG-PET negative patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003006-29 | Sponsor Protocol Number: A0081072 | Start Date*: 2005-09-26 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Trial of the Anxiolytic Efficacy of Pregabalin and Alprazolam IR in Subjects with Anxiety prior to Dental Procedure | |||||||||||||
Medical condition: Anxiety prior to Dental Procedure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005059-32 | Sponsor Protocol Number: MDX010-20 | Start Date*: 2005-10-07 |
Sponsor Name:Medarex, Inc. | ||
Full Title: A Randomized, Double-Blind, Multicenter Study Comparing MDX-010 Monotherapy, MDX-010 in Combination with a Melanoma Peptide Vaccine, and Melanoma Peptide Vaccine Monotherapy in HLA-A*0201-Positive ... | ||
Medical condition: HLA-A*0201-Positive Patients with Previously Treated, Unresectable Stage III or IV Melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) BE (Completed) HU (Completed) | ||
Trial results: View results |
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