- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,380 result(s) found.
Displaying page 525 of 2,219.
| EudraCT Number: 2013-005529-22 | Sponsor Protocol Number: H-6-2013-011 | Start Date*: 2014-03-21 | ||||||||||||||||
| Sponsor Name:Rigshospitalet | ||||||||||||||||||
| Full Title: Platelet inhibition in comatose patients receiving oral anti platelet therapy through a naso-gastric tube after undergoing acute percutaneous coronary intervention | ||||||||||||||||||
| Medical condition: Patients surviving cardiac arrest and undergoing percutaneous coronary intervention | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-005569-38 | Sponsor Protocol Number: CLS003-CO-PR-001 | Start Date*: 2014-02-17 | |||||||||||
| Sponsor Name:Cutanea Life Sciences | |||||||||||||
| Full Title: A phase I/IIa open-label First-in-Human study to assess safety and pharmacokinetics and explore biomarker effects of topical ionic contra-viral therapy (ICVT) comprised of digoxin and furosemide in... | |||||||||||||
| Medical condition: Cutaneous warts | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003896-20 | Sponsor Protocol Number: 3667 | Start Date*: 2013-02-14 |
| Sponsor Name:The Royal Marsden NHS Foundation Trust [...] | ||
| Full Title: TAX-TORC: A Phase I multi-centre trial of the combination of AZD2014 (dual TORC1 and TORC2 inhibitor) and weekly paclitaxel in patients with solid tumours | ||
| Medical condition: Solid tumours | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003942-33 | Sponsor Protocol Number: M13-796 | Start Date*: 2013-05-03 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prevention of Acute Kidney Injury in Subjects Undergoing High Risk... | |||||||||||||
| Medical condition: Acute Kidney Injury | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000359-42 | Sponsor Protocol Number: ML28695 | Start Date*: 2013-09-12 | |||||||||||
| Sponsor Name:ROCHE HELLAS S.A. | |||||||||||||
| Full Title: Multicenter, open label, phase IIIb study to evaluate the safety and tolerability of subcutaneous tocilizumab as monotherapy and/or in combination with methotrexate or other non-biologic disease mo... | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000364-28 | Sponsor Protocol Number: 00/0594-LINARI | Start Date*: 2013-05-16 | |||||||||||
| Sponsor Name:Profil Institut für Stoffwechselforschung GmbH | |||||||||||||
| Full Title: Effects of Linagliptin on active GLP-1 concentrations in subjects with renal impairment | |||||||||||||
| Medical condition: Type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004403-13 | Sponsor Protocol Number: PDT002/12 | Start Date*: 2013-08-27 |
| Sponsor Name:Medizinische Universität Wien, Univ. Klinik für Dermatologie | ||
| Full Title: Placebo-controlled cross-over study on the efficacy of a non-steroidal antirheumatic drug for pain reduction during photodynamic therapy of actinic keratoses | ||
| Medical condition: actinic keratosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004770-25 | Sponsor Protocol Number: CLOTILDIA | Start Date*: 2012-10-30 | |||||||||||
| Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
| Full Title: CLOpidogrel versus TIcagreLor for antiplatelet maintenance in DIAbetic patients (CLOTILDIA) | |||||||||||||
| Medical condition: patients with type 2 diabetes mellitus and known coronary artery disease on dual antiplatelet therapy (aspirin 100 mg qd and clopidogrel 75 mg qd) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000801-21 | Sponsor Protocol Number: 20130218 | Start Date*: 2014-08-26 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Stimulation of the ovaries in women with breast cancer undergoing fertility preservation: alternative versus standard stimulation protocols; the STIM-trial | ||
| Medical condition: Ovarian stimulation in women with breast cancer prior to chemotherapy | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-000819-25 | Sponsor Protocol Number: 43712 | Start Date*: 2013-10-22 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Autologous BM derived MSCs in combination with everolimus to preserve renal structure and function in renal recipients | ||
| Medical condition: renal recipients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-000858-22 | Sponsor Protocol Number: AFLIBC06561 | Start Date*: 2013-09-12 | |||||||||||
| Sponsor Name:Sanofi-Aventis Groupe | |||||||||||||
| Full Title: A Single-Arm, Open Label Study of Aflibercept as Maintenance Therapy Following Induction with Aflibercept in Combination with XELOX, as First-Line Treatment for Metastatic Colorectal Cancer Patient | |||||||||||||
| Medical condition: Colorectal cancer metastatic | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003582-25 | Sponsor Protocol Number: NL59128 | Start Date*: 2017-01-23 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: The added effect of oral ondansetron to care-as-usual on persisting vomiting in children aged 6 months to 6 years, presenting at primary care out of hours service with acute gastro-enteritis and co... | ||
| Medical condition: Gastroenteritis | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001369-28 | Sponsor Protocol Number: 880 | Start Date*: 2014-10-30 | |||||||||||
| Sponsor Name:Gateshead Health NHS Foundation Trust | |||||||||||||
| Full Title: THYRoxine in Acute Myocardial Infarction (ThyrAMI) | |||||||||||||
| Medical condition: Hypothyroidism and Acute Myocardial Infarction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001435-13 | Sponsor Protocol Number: CHUBX2014/22 | Start Date*: 2016-05-19 |
| Sponsor Name:CHU de Bordeaux | ||
| Full Title: Description of the ability to learn how to handle inhaler devices in COPD | ||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001421-41 | Sponsor Protocol Number: TWOProtocolv1.0 | Start Date*: 2018-05-22 | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: The TWO Study: Transplantation Without Over-immunosuppression. A Phase IIb Trial of Regulatory T Cells in Renal Transplantation. | |||||||||||||
| Medical condition: Renal (allograft) transplant | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001174-34 | Sponsor Protocol Number: B1851140 | Start Date*: 2016-07-13 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A PHASE 4/3, OPEN-LABEL, SINGLE-ARM, MULTICENTER STUDY TO DESCRIBE THE SAFETY AND IMMUNOGENICITY OF 13-VALENT PNEUMOCOCCAL CONJUGATE VACCINE IN ADULTS 50 TO 65 YEARS OF AGE AND IN CHILDREN 6 TO 17 ... | |||||||||||||
| Medical condition: Pneumococcal infection | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002426-70 | Sponsor Protocol Number: 104005 | Start Date*: 2015-06-01 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: Phase III b, open, randomised, multicenter study to evaluate the immunogenicity and safety of GlaxoSmithKline Biologicals’ combined diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated po... | ||
| Medical condition: Primary immunisation of healthy infants in the first year of life against diphtheria, tetanus, pertussis, hepatitis B, polio, Haemophilus influenzae type b diseases. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004662-26 | Sponsor Protocol Number: LACAC_L_04298 | Start Date*: 2015-03-25 | |||||||||||
| Sponsor Name:Sanofi | |||||||||||||
| Full Title: Safety Dermatological Evaluation: genital Mucosa Irritation - Product tested: Dermacyd PH_DETINLYN Sweet Flower. | |||||||||||||
| Medical condition: Healthy volunteers (hygiene) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003386-22 | Sponsor Protocol Number: PRX302-2-07 | Start Date*: 2015-01-19 |
| Sponsor Name:Sophiris Bio Corp | ||
| Full Title: A Single Centre, Open Label, Phase IIa Study, Evaluating the Safety and Tolerability of Targeted Intraprostatic Administration of PRX302 to Treat Men with Histologically Proven, Clinically Signific... | ||
| Medical condition: Prostate cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001941-25 | Sponsor Protocol Number: 2014-002 | Start Date*: 2014-12-16 | |||||||||||||||||||||
| Sponsor Name:Rigshospitalet 2121 | |||||||||||||||||||||||
| Full Title: Pilot Study with Treatment of Short Bowel Syndrome Patients with dipeptidyl-peptidase 4 inhibitor, Sitagliptin (Januvia®) | |||||||||||||||||||||||
| Medical condition: Short Bowel Syndrome with intestinal failure (SBS IF) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
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