- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Coefficient of variation.
Displaying page 1 of 3.
EudraCT Number: 2010-018781-23 | Sponsor Protocol Number: 2917800009 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Top Institute Food and Nutrition | |||||||||||||
Full Title: Diagnose of GH-deficiency: comparing the dietary-protein test with conventional Growth Hormone Stimulation Tests | |||||||||||||
Medical condition: To investigate if there is a correlation between the peak GH concentrations after ingestion of gelatin protein and the peak GH concentrations after the two standard tests (GHST) in order to discrim... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003941-41 | Sponsor Protocol Number: ABR46374 | Start Date*: 2013-11-07 |
Sponsor Name:Medisch Spectrum Twente | ||
Full Title: Reversibility of pulmonary function after inhaling salbutamol in different doses in standard and forward leaning body posture in asthmatic children | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
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: 2021-003777-63 | Sponsor Protocol Number: 202100482 | Start Date*: Information not available in EudraCT |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Tetrahydrobiopterin (BH4) treatment in Phenylketonuria - comparing different practices of dosing regimen | ||
Medical condition: Phenylketonuria (PKU; OMIM 261600) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003981-42 | Sponsor Protocol Number: 2012.2708 | Start Date*: 2014-10-20 |
Sponsor Name:University Medical Center Groningen [...] | ||
Full Title: Estrogen receptor and androgen receptor imaging in metastatic breast cancer patients | ||
Medical condition: Estrogen receptor positive metastatic breast cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
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: 2012-003790-25 | Sponsor Protocol Number: 12AR04 | Start Date*: 2012-12-21 |
Sponsor Name:Great Ormond Street Hospital for Children NHS Foundation Trust | ||
Full Title: Comparison of measured versus predicted blood propofol concentrations in children undergoing spinal surgery | ||
Medical condition: Children undergoing spinal surgery have propofol anaesthesia delivered by a computerised syringe driver (Target Controlled Infusion or TCI). Spinal surgery is associated with major blood loss. This... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003581-26 | Sponsor Protocol Number: DuoCOMT2008-05-27 | Start Date*: 2008-07-18 | |||||||||||
Sponsor Name:Dept of Neuroscience, Uppsala University | |||||||||||||
Full Title: Pharmacokinetics of levodopa using duodenal levodopa/carbidopa infusion with and without oral COMT inhibitors | |||||||||||||
Medical condition: Parkinson's disease (G20.9), advanced, patients presently on Duodopa treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006280-21 | Sponsor Protocol Number: CORIOLAN | Start Date*: 2012-04-27 | ||||||||||||||||
Sponsor Name:Jules Bordet Institute | ||||||||||||||||||
Full Title: Correlating the tumoral metabolic progression index measured by serial FDG PET-CT and apparent diffusion coefficient measured by MRI to patient's outcome in advance colorectal cancer | ||||||||||||||||||
Medical condition: Advanced colorectal cancer, refractory to all available medications | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-005684-32 | Sponsor Protocol Number: | Start Date*: 2015-12-30 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: [18F] DIHYDRO-TESTOSTERONE PET IMAGING IN PATIENTS WITH PROGRESSIVE PROSTATE CANCER | |||||||||||||
Medical condition: Progressive Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002756-91 | Sponsor Protocol Number: LPS14947 | Start Date*: 2019-10-24 | |||||||||||
Sponsor Name:Sanofi Aventis Groupe | |||||||||||||
Full Title: A 12-week randomized, controlled trial to compare TOUJEO® and TRESIBA® in terms of glucose values in target range and variability during continuous glucose monitoring in patients with type 1 diabet... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002028-26 | Sponsor Protocol Number: AK0529-1003 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Ark Biosciences Pty Ltd. | |||||||||||||
Full Title: A Randomised, Double-blind, Placebo-controlled, 2-Part Study of Orally Administered AK0529 to Evaluate the Safety, Tolerability, Pharmacokinetics and Antiviral Effect of Single and Multiple Dosing ... | |||||||||||||
Medical condition: Respiratory Syncytial Virus Infection | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001912-21 | Sponsor Protocol Number: caih | Start Date*: 2007-06-26 | |||||||||||
Sponsor Name:Aarhus Sygehus, Universityhospital of Aarhus | |||||||||||||
Full Title: Bioavailability, Pharmacokinetics and Pharmacodynamics of Insulin Aspart following Subcutaneous Insulin Infusion (CSII) - Basal Rate Resolution. | |||||||||||||
Medical condition: Type 1 diabetes mellitus Continious subcutaneous insulin infusion (CSII) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006967-35 | Sponsor Protocol Number: HEME 1.0 | Start Date*: 2009-02-11 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für klinische Pharmakologie | |||||||||||||
Full Title: The effects of intravenous heme arginate on functional magnetic resonance imaging during ischemia | |||||||||||||
Medical condition: ischemia reperfusion injury | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003710-13 | Sponsor Protocol Number: Pro-Tac | Start Date*: Information not available in EudraCT |
Sponsor Name:University Hospital Essen | ||
Full Title: A multi-center interventional study to assess pharmacokinetics, effectiveness and tolerability of prolonged-release Tacrolimus after Paediatric Kidney Transplantation | ||
Medical condition: Caucasian paediatric kidney transplant recipients | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001956-40 | Sponsor Protocol Number: PK_pregnancy | Start Date*: 2023-03-05 |
Sponsor Name:Medical University Vienna | ||
Full Title: Antibiotic pharmacokinetics in women with twin pregnancy | ||
Medical condition: The target population are twin pregnancy women that will deliver through c-section and that are receiving one or more of the included antibiotics. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002008-33 | Sponsor Protocol Number: A6181196 | Start Date*: 2012-02-21 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE I/II STUDY OF SUNITINIB IN YOUNG PATIENTS WITH ADVANCED GASTROINTESTINAL STROMAL TUMOR | |||||||||||||
Medical condition: Pediatric Gastro Intestinal Stromal Tumor (GIST) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) Outside EU/EEA CZ (Completed) PT (Completed) IT (Completed) GB (Completed) PL (Completed) AT (Completed) DE (Completed) FR (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004684-58 | Sponsor Protocol Number: FE 200486 CS24 | Start Date*: 2007-01-08 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, assessor-blind, parallel groups, multi-centre, exploratory study assessing the impact of subcutaneous administration of degarelix 2.5 mg on synchronisation of follicle cohort compared... | |||||||||||||
Medical condition: Prevention of premature luteinizing hormone (LH) surges in women undergoing controlled ovarian hyperstimulation for assisted reproductive technologies (ART) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002920-10 | Sponsor Protocol Number: TRE-1486--0105-I | Start Date*: 2016-09-14 |
Sponsor Name:Klinikum der Universitaet Muenchen AoeR | ||
Full Title: TREAT-SVDs: EffecTs of Amlodipine and other Blood PREssure Lowering Agents on Microvascular FuncTion in Small Vessel Diseases | ||
Medical condition: Cerebral small vessel disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) NL (Ongoing) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000384-24 | Sponsor Protocol Number: DB2114956 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 4-Week Randomized Cross-Over Study to Evaluate Daily Lung Function Following the Administration of Albuterol/Salbutamol and Ipratropium in Subjects with Chronic Obstructive Pulmonary Disease | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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