- Trials with a EudraCT protocol (11,266)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11,266 result(s) found for: Test Two.
Displaying page 138 of 564.
| EudraCT Number: 2015-003534-27 | Sponsor Protocol Number: CIGE025B1301 | Start Date*: 2016-02-16 |
| Sponsor Name:Novartis Pharmaceuticals | ||
| Full Title: A 24 Week, Open Label, Multi-center Evaluation of Pharmacokinetics and Pharmacodynamics, Efficacy and Safety of Omalizumab in Japanese Children (6 - 15 Years) With Inadequately Controlled Allergic ... | ||
| Medical condition: Allergic asthma | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2015-005339-42 | Sponsor Protocol Number: N16HPV | Start Date*: 2016-08-30 |
| Sponsor Name:NKI-AVL | ||
| Full Title: Safety, immunogenicity and clinical response of sig-HELP-E6SH/E7SH-kdel, injected in the epidermis by DNA tattoo, in HPV16-positive vulvar intraepithelial neoplasia: a phase I/II study | ||
| Medical condition: HPV16+ usual type vulvar intraepithelial neoplasia (uVIN) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001455-40 | Sponsor Protocol Number: GRECCO-19 | Start Date*: 2020-04-01 | |||||||||||
| Sponsor Name:Hellenic Society of Rhythmology | |||||||||||||
| Full Title: The Greek study in the Effects of Colchicine in Covid-19 complications prevention | |||||||||||||
| Medical condition: This trial will investigate if colchicine could potentially have an effect in patients’ clinical course by limiting the myocardial necrosis and pneumonia development in the context of COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003959-29 | Sponsor Protocol Number: 2016RKH | Start Date*: 2016-11-10 | |||||||||||
| Sponsor Name:Helena Tinkanen, Tampereen yliopistollinen sairaala | |||||||||||||
| Full Title: Scientific title: A Protocol for a Randomized, Two-Parallel-group Study to Compare the Efficacy of Testing LH Surge at Home Versus Medically Triggered Ovulation with hCG (Pregnyl®) in the Naturally... | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003010-26 | Sponsor Protocol Number: B076201627677 | Start Date*: 2018-01-11 |
| Sponsor Name:Centre Hospitalier Universitaire Saint Pierre , ULB | ||
| Full Title: Hyperbaric Bupivacaine Versus Hyperbaric Prilocaine 2% for Cesarean Section Under Spinal Anesthesia: a Randomised and Controlled Clinical Trial | ||
| Medical condition: Parturients undergoing an elective caesarean section performed under spinal anaesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001681-25 | Sponsor Protocol Number: 23681 | Start Date*: 2015-07-15 |
| Sponsor Name:Merck KGaA | ||
| Full Title: An Open, Multicenter, Randomized, Controlled Trial to Evaluate the Correlation Between Spontaneous Catch-up Growth, Clinical Response to Saizen (Recombinant Human Growth Hormone, r-hGH) and Gene Ex... | ||
| Medical condition: Small for Gestational Age | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000248-32 | Sponsor Protocol Number: CICL670F2102 | Start Date*: 2016-03-15 |
| Sponsor Name:Novartis Pharmaceuticals Corporation | ||
| Full Title: A randomized, open-label, single center, phase I, cross-over study to evaluate the pharmacokinetic comparability of deferasirox new tablet formulation with the reference dispersible formulation in ... | ||
| Medical condition: Healthy subjects | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2011-004201-25 | Sponsor Protocol Number: 1B | Start Date*: 2011-11-30 |
| Sponsor Name:Erasmus MC | ||
| Full Title: The BOKITO-1B Study: Tenofovir DF Bone and Kidney Toxicity. Pharmacology in HBV monoinfected patients. | ||
| Medical condition: Chronic hepatitis B | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004354-28 | Sponsor Protocol Number: S-20120017 | Start Date*: 2013-07-02 |
| Sponsor Name:Børneafdelingen Kolding | ||
| Full Title: Maintenance treatment in childhood constipation. A randomized placebo-controlled intervention study | ||
| Medical condition: Childhood functional constipation. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002415-10 | Sponsor Protocol Number: PROCoMBO | Start Date*: 2014-02-11 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: [18F]-labelled FDHT in PET/CT for detection and staging of bone metastases in hormone naïve prostate cancer | ||
| Medical condition: Hormone naive prostate cancer, metastasized to bone (2 or more bone metastases). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001440-38 | Sponsor Protocol Number: 42647 | Start Date*: 2014-05-22 | |||||||||||
| Sponsor Name:Department of Dermatology D92, Bispebjerg Hospital | |||||||||||||
| Full Title: Methods to increase PpIX formation in the skin of healthy volunteers | |||||||||||||
| Medical condition: Healthy volunteers - no medical condition is investigated but pharmaco kinetics | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002906-38 | Sponsor Protocol Number: 58525 | Start Date*: 2016-10-12 |
| Sponsor Name:MC Slotervaart | ||
| Full Title: Reducing pain and discomfort during and after bone marrow aspiration | ||
| Medical condition: Pain and fear reduction for bone marrow examination | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002160-17 | Sponsor Protocol Number: Lidospray1 | Start Date*: 2016-06-24 |
| Sponsor Name:Diana Molina Villaverde | ||
| Full Title: UNICENTER RANDOMIZED SIMPLE BLIND CLINICAL TRIAL TO COMPARE THE EFFECTIVENESS OF LIDOCAINE SPRAY VERSUS CONVENTIONAL ANALGESIA WHILE CURES IN PATIENTS WITH COMPLEX SURGICAL WOUNDS | ||
| Medical condition: analyse whether patients with intravenous analgesic treatment will have the same degree of pain that patients with the same pattern of analgesia, they make a topical application of lidocaine 2% dur... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001222-42 | Sponsor Protocol Number: CAPSS-272 | Start Date*: 2015-04-24 |
| Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development, L.L.C. | ||
| Full Title: A double-blind trial comparing the efficacy, tolerability and safety of monotherapy topiramate versus phenytoin in subjects with seizures indicative of new onset epilepsy | ||
| Medical condition: New onset epilepsy | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002064-15 | Sponsor Protocol Number: 66176 | Start Date*: 2019-04-15 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Treatment of Perianal FIstulas in Crohn’s Disease: Surgical closure vs Anti-TNF | ||
| Medical condition: Perianal fistulas in Crohn's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004063-31 | Sponsor Protocol Number: FIM-PRELEVD-2018-01 | Start Date*: 2019-04-26 |
| Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud (FIMABIS) | ||
| Full Title: Mechanisms of cardio and nephroprotection in patients who are going on cardiac surgery with right ventricular dysfunction, with preoperative treatment of levosimendan compared with placebo. (PREL... | ||
| Medical condition: Perioperative right ventricle dysfunction | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001059-63 | Sponsor Protocol Number: 2015.009 | Start Date*: 2015-09-23 | |||||||||||
| Sponsor Name:Aalborg University | |||||||||||||
| Full Title: BONATHIAD - Bone Association with Thiazide Diuretics. | |||||||||||||
| Medical condition: The effect of bendroflumethiazide with potassium supplement when used as an adjuvant to oral bisphosphonates in the treatment of newly diagnosed osteoporosis among post-menopausal women above 50 ye... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004776-20 | Sponsor Protocol Number: BAP00626 | Start Date*: 2006-03-27 |
| Sponsor Name:Basilea Pharmaceutica Ltd | ||
| Full Title: Safety and Efficacy of Alitretinoin in the Treatment of Severe Refractory Chronic Hand Dermatitis | ||
| Medical condition: Severe Chronic Hand Dermatitis (CHaD) Refractory to Topical Therapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011531-13 | Sponsor Protocol Number: ICSR | Start Date*: 2009-08-04 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: Relative adrenal insufficiency in cirrhosis: relevance in patients with ascites and treatment with hydrocortisone in refractory ascites | |||||||||||||
| Medical condition: cirrhosis and ascites | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-008689-11 | Sponsor Protocol Number: 3/15.12.2008 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Children's Memorial Health Institute | ||
| Full Title: Efficacy and safety of omega – 3 based lipid solution (Omegaven) in comparison with Lipofundin LCT/MCT in reducing cholestasis in children on parenteral nutrition – randomized double – blind clinic... | ||
| Medical condition: Parenteral nutrition associated liver disease (PNALD) MedDRA LLT: total parenteral nutrition MedDRA PT: parenteral nutrition MedDRA LLT: liver cholestasis MedDRA PT: cholestasis | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: PL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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