- Trials with a EudraCT protocol (409)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (189)
409 result(s) found for: Observational study.
Displaying page 9 of 21.
EudraCT Number: 2016-001357-40 | Sponsor Protocol Number: HDZNRW-KA_006_TB | Start Date*: 2016-11-08 |
Sponsor Name:Klinik für Kardiologie, Herz- und Diabeteszentrum NRW | ||
Full Title: High-Flow-Therapy for the treatment of Cheyne-Stokes-Respiration in chronic heart failure: A randomized, controlled, cross-over trial | ||
Medical condition: Cheyne-Stokes Respiration in chronic heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-002185-23 | Sponsor Protocol Number: DIPG | Start Date*: 2015-07-29 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Phase 2 open label randomized study of radiotherapy, concomitant nimotuzumab and vinorelbine and re-irradiation at relapse versus radiotherapy and multiple elective radiotherapy courses with concom... | |||||||||||||
Medical condition: diffuse intrinsic pontine glioma | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2025-000106-42 | Sponsor Protocol Number: 213560 | Start Date*: 2025-04-22 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: Protocol Title: A Multi-Center, Open-Label Study to Evaluate Safety, Efficacy and Pharmacokinetics of Belimumab Plus Standard Therapy in Chinese Paediatric Patients with Active Systemic Lupus Eryth... | ||
Medical condition: Active Systemic Lupus Erythematosus (SLE) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2006-004708-38 | Sponsor Protocol Number: 1326 | Start Date*: 2006-08-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ISTITUTI OSPITALIERI DI VERONA | |||||||||||||
Full Title: Randomized evaluation of the effectiveness of clozapine and aripiprazole versus clozapine and haloperidol in the treatment of schizofrenia. An independent, pragmatic, multicentre, parallel-group, s... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000719-19 | Sponsor Protocol Number: 09/100/10 | Start Date*: 2011-05-05 |
Sponsor Name:University of Birmingham | ||
Full Title: A Randomised Controlled Trial of the Efficacy and Mechanism of Levothyroxine Treatment on Pregnancy and Neonatal Outcomes in Women with Thyroid Antibodies. (TABLET: Thyroid AntiBodies and LEvoThyro... | ||
Medical condition: Thyroid autoimmunity and history of miscarriage or infertility. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006562-42 | Sponsor Protocol Number: RD-5103-007-06 | Start Date*: 2008-02-21 | |||||||||||
Sponsor Name:Derby Hospitals NHS Foundation Trust | |||||||||||||
Full Title: An Observational and Exploratory Study to determine the effect of anti TNF Biologic Treatment in Rheumatoid Cachexia | |||||||||||||
Medical condition: Cachexia in patients with Rheumatoid arthritis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002348-42 | Sponsor Protocol Number: RG_13-151 | Start Date*: 2014-12-10 |
Sponsor Name:University of Birmingham | ||
Full Title: Effectiveness of progesterone to prevent miscarriage in women with early pregnancy bleeding: A randomised placebo-controlled trial (PRISM Trial: PRogesterone In Spontaneous Miscarriage Trial) | ||
Medical condition: Vaginal bleeding in the first 12 weeks of pregnancy. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002470-42 | Sponsor Protocol Number: FluSHED-2 | Start Date*: 2018-08-30 | |||||||||||
Sponsor Name:Imperial College London JRC Office | |||||||||||||
Full Title: Assessment of viral shedding week following administration of live attenuated influenza vaccine in children: FluSHED-2 study | |||||||||||||
Medical condition: Prevention of influenza infection through immunisation | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000444-22 | Sponsor Protocol Number: NL75930.078.20 | Start Date*: 2021-04-07 |
Sponsor Name:Erasmus MC | ||
Full Title: Differences in coagulation between fresh frozen plasma and Solventdetergent plasma in pediatric congenital heart surgery | ||
Medical condition: coagulation in pediatric cardiac surgery | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011893-13 | Sponsor Protocol Number: 1234567899 | Start Date*: 2010-04-29 |
Sponsor Name:Isala Klinieken | ||
Full Title: Adherence of antidepressants during pregnancy | ||
Medical condition: Pregnant women with psychiatric morbidity and an strong indication for using antidepressants | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005844-32 | Sponsor Protocol Number: Td9805-LT | Start Date*: 2016-01-26 | |||||||||||||||||||||
Sponsor Name:Sanofi Pasteur Limited | |||||||||||||||||||||||
Full Title: One-, Three-, Five- and Ten-Year Data on the Long-Term Immunogenicity of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (Tdap) in Adolescents 11–14 Years of Age | |||||||||||||||||||||||
Medical condition: Active immunization against tetanus, diphtheria and pertussis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000909-24 | Sponsor Protocol Number: 201302-OPTICLOT | Start Date*: 2013-08-29 | |||||||||||||||||||||
Sponsor Name:Erasmus MC | |||||||||||||||||||||||
Full Title: "OPTI-CLOT": Peri-Operative PharmacokineTIc-guided dosing of CLOTting factor in Hemophilia. | |||||||||||||||||||||||
Medical condition: Hemophillia | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001193-81 | Sponsor Protocol Number: EGIS-SCH-02-2006 | Start Date*: 2007-05-17 |
Sponsor Name:EGIS Gyógyszergyár Nyrt. | ||
Full Title: KETILEPT® hatékonyságának és biztonságosságának ellenőrzése szkizofrénia és szkizoaffektiv betegség akut epizódjának kezelésében, multicentrikus, nyílt, megfigyeléses vizsgálatban (Controll of... | ||
Medical condition: Ez a tervezett tanulmány a generikus quetiapin hatékonyságának és biztonságosságának vizsgálatát tűzte ki célul, mert fontos, hogy a generikus készítmények valódi tulajdonságairól is legyenek infor... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001539-29 | Sponsor Protocol Number: alsbjerg1 | Start Date*: 2019-10-11 | |||||||||||
Sponsor Name:The Fertility Clinic, Skive Regional Hospital | |||||||||||||
Full Title: Optimizing serum progesterone level during luteal phase in hormone replacement therapy frozen embryo transfer (HRT-FET) cycle – interventional and observational trial | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002259-20 | Sponsor Protocol Number: CASUAL_ECMO | Start Date*: 2023-08-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: A three-arm randomized controlled non-inferiority pilot study Comparing Anticoagulation Strategies using Unfractionated heparin, Argatroban and Low-molecular-weight heparin for Extracorporeal Memb... | ||
Medical condition: patients with indication for extracorporeal membrane oxygenation therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005065-31 | Sponsor Protocol Number: 9769 | Start Date*: 2017-05-09 |
Sponsor Name:University hospital of Montpellier | ||
Full Title: Comparison of preoperative hemoglobin after administration of epoetin alpha associated with oral martial supplementation vs intraveinous martial supplementation before craniosynostosis in children | ||
Medical condition: Craniosynostosis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003687-52 | Sponsor Protocol Number: M13-961 | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-Blind, Controlled Study to Evaluate the Efficacy and Safety of the Combination of ABT-450/Ritonavir/ABT-267 (ABT 450/r/ABT-267) and ABT-333 With and Without Ribavirin (RBV) in ... | |||||||||||||
Medical condition: Chronic Hepatitis C Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) BE (Completed) HU (Completed) AT (Completed) IT (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001384-23 | Sponsor Protocol Number: 65512-SAFESTOP | Start Date*: 2018-11-08 | |||||||||||
Sponsor Name:Erasmus Medical Center | |||||||||||||
Full Title: Safe Stop Trial: observational study of the STOP & GO strategy of PD-1 blockade in advanced melanoma patients upon achieving a complete or partial response | |||||||||||||
Medical condition: malignant and not otherwise specified skin neoplasms | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006751-48 | Sponsor Protocol Number: 08/0170 | Start Date*: 2009-08-12 | |||||||||||
Sponsor Name:University College London [...] | |||||||||||||
Full Title: PHASE II STUDY OF BORTEZOMIB CONSOLIDATION AFTER HIGH DOSE THERAPY AND AUTOLOGOUS STEM CELL TRANSPLANTATION FOR MULTIPLE MYELOMA | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000087-42 | Sponsor Protocol Number: TAISTR_2016 | Start Date*: 2016-05-11 |
Sponsor Name:University College Dublin | ||
Full Title: A multicentre, prospective, single arm, open-label 96 week observational trial of the tolerability, adherence and efficacy of a dolutegravir/abacavir/lamivudine single tablet regimen in HIV-1 antib... | ||
Medical condition: Human Immunodeficiency Virus (HIV) infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
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