- Trials with a EudraCT protocol (44,400)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,400 result(s) found.
Displaying page 5 of 2,220.
| EudraCT Number: 2016-002112-41 | Sponsor Protocol Number: 2016-05-04 | Start Date*: 2016-07-16 |
| Sponsor Name:Region Östergötland | ||
| Full Title: Can Insuline improve the healing of dental implants? | ||
| Medical condition: Missing teeth | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001264-11 | Sponsor Protocol Number: UMCM-2016EPI05 | Start Date*: 2016-09-07 |
| Sponsor Name:University Medical Center of the Johannes Gutenberg-University Mainz | ||
| Full Title: A phase IV, single-center, randomized, double-blind, placebo-controlled, parallel group study on the effects of empagliflozin on left ventricular diastolic function compared to usual care in indivi... | ||
| Medical condition: Poorly controlled type 2 diabetes mellitus in adults | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003937-62 | Sponsor Protocol Number: CLR_16_23 | Start Date*: 2017-03-20 | |||||||||||
| Sponsor Name:SUN Pharma Global FZE | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multiple Dose, Phase 2b Study to Demonstrate the Safety and Efficacy of Tildrakizumab in Subjects with Active Psoriatic Arthritis | |||||||||||||
| Medical condition: Psoriatic Arthritis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-005111-40 | Sponsor Protocol Number: CN138-178 | Start Date*: 2017-04-07 |
| Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc | ||
| Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Flexible- Dosed Parallel-Group Study of Aripiprazole Flexibly Dosed in the Treatment of Children and Adolescents with Autistic Disorder | ||
| Medical condition: Autistic Disorder | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000611-17 | Sponsor Protocol Number: LTS12745 | Start Date*: 2017-08-28 | |||||||||||
| Sponsor Name:Alfresa Pharma Corporation and Sanofi KK | |||||||||||||
| Full Title: A Long term study of M071754 - A open-label study in patients with infantile spasms. | |||||||||||||
| Medical condition: Patients diagnosed with infantile spasms | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000608-14 | Sponsor Protocol Number: 1.0/170119 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Tartu University Hospital | ||
| Full Title: Prospective validation of individualized Bayesian dose optimization tool DosOpt for Vancomycin treatment in neonates. | ||
| Medical condition: In neonatal population wide inter-and intra-individual variability of pharmacokinetics makes extremely difficult to ensure optimal exposure of vancomycin with standard regimens. On average >50% of ... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
| Trial protocol: EE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000608-27 | Sponsor Protocol Number: ProtokolSB2 | Start Date*: 2016-04-05 | |||||||||||||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
| Full Title: The effect of subsartorial saphenous block on postoperative pain following major ankle and hind foot surgery | |||||||||||||||||||||||
| Medical condition: Post-operative pain after four types of major ankle and hind foot surgery: (1) total ankle arthroplasty, (2) ankle arthrodesis, (3) subtalar arthrodesis or (4) triple arthrodesis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2014-003833-24 | Sponsor Protocol Number: AGMT_HNO_PN | Start Date*: 2016-06-30 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:AGMT – Arbeitsgemeinschaft medikamentöse Tumortherapie gemeinnützige GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Randomized phase III study: Supplemental parenteral nutrition for patients with locally advanced inoperable tumors of the head and neck, receiving definitive radiotherapy with Cetuximab or Cisplatin | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced inoperable tumors of the head and neck under definitive radiotherapy with Cetuximab or Cisplatin | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-000473-20 | Sponsor Protocol Number: CLCZ696B3402 | Start Date*: 2016-08-18 | |||||||||||
| Sponsor Name:Novartis Pharma services AG | |||||||||||||
| Full Title: A prospective evaluation of natriuretic peptide based referral of CHF patients in primary care | |||||||||||||
| Medical condition: Chronic heart failure with reduced ejection fraction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003629-13 | Sponsor Protocol Number: PROFIT | Start Date*: 2018-01-31 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: A Prospective, randomised placebo controlled feasibility trial of Faecal Microbiotica Transplantation in cirrhosis | |||||||||||||
| Medical condition: Cirrhosis of the liver | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001974-27 | Sponsor Protocol Number: STOPFLU | Start Date*: 2019-10-15 | |||||||||||||||||||||
| Sponsor Name:Centre Hospitalier Universitaire Vaudois (CHUV) | |||||||||||||||||||||||
| Full Title: Reducing the Burden of Influenza after Solid-Organ Transplantation: the STOP-FLU trial [Swiss Trial in solid Organ transplantation on Prevention of inFLUenza] | |||||||||||||||||||||||
| Medical condition: Influenza in solid organ transplant patients | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2019-002956-18 | Sponsor Protocol Number: ZWI-ZW25-202 | Start Date*: 2020-03-25 |
| Sponsor Name:Zymeworks Inc. | ||
| Full Title: Phase 2a Study of ZW25 in Combination with Palbociclib Plus Fulvestrant | ||
| Medical condition: Breast cancer patients including those with locally advanced (unresectable) or metastatic HER2-positive, HR-positive breast cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001586-87 | Sponsor Protocol Number: RSLV-132-04 | Start Date*: 2016-09-29 |
| Sponsor Name:Resolve Therapeutics, LLC | ||
| Full Title: A Phase 2, Double Blind, Placebo Controlled Study of RSLV-132 in Subjects with Primary Sjogren’s Syndrome | ||
| Medical condition: Primary Sjogrens Syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003248-34 | Sponsor Protocol Number: IMPAACTP1110 | Start Date*: 2016-11-02 | |||||||||||
| Sponsor Name:NIAID and NICHD | |||||||||||||
| Full Title: A PHASE I TRIAL TO EVALUATE THE SAFETY AND PHARMACOKINETICS OF RALTEGRAVIR IN HIV-1-EXPOSED NEONATES AT HIGH RISK OF ACQUIRING HIV-1 INFECTION | |||||||||||||
| Medical condition: New born babies at risk of acquiring HIV from their infected mothers. | |||||||||||||
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| Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000755-97 | Sponsor Protocol Number: EPFL-CNBI-2017-01 | Start Date*: 2017-03-16 |
| Sponsor Name:Defitech Chair in Brain-Machine Interface, EPFL | ||
| Full Title: Brain-computer interface and neuromuscular stimulation for rehabilitation following chronic stroke | ||
| Medical condition: I61 - Intracerebral haemorrhage I63 - Cerebral infarction Chronic condition (at least 10 months after occurrence of cerebrovascular accident) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004903-33 | Sponsor Protocol Number: IBM4809 | Start Date*: 2018-06-18 | |||||||||||
| Sponsor Name:Orphazyme A/S | |||||||||||||
| Full Title: Phase 2/3 Study of Arimoclomol in Inclusion Body Myositis (IBM) A Randomized, Double-blind, Placebo-Controlled Trial | |||||||||||||
| Medical condition: Sporadic Inclusion Body Myositis (sIBM) | |||||||||||||
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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: 2019-003486-17 | Sponsor Protocol Number: 9-VPH-MVIH | Start Date*: 2020-02-11 |
| Sponsor Name:CARMEN HIDALGO TENORIO | ||
| Full Title: Immunogenicity and safety of a 9-valent human papillomavirus vaccine in HIV-positive women | ||
| Medical condition: New infection and lesions of papillomavirus in HIV-infected women | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002296-18 | Sponsor Protocol Number: CaTo-ROC | Start Date*: 2015-07-30 | |||||||||||
| Sponsor Name:Vejle Hospital, Department of Oncology | |||||||||||||
| Full Title: Cabazitaxel in patients with Recurrent Ovarian Cancer after failure of standard therapy- A phase II trial | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000605-20 | Sponsor Protocol Number: FFIS/2017/01/SLT | Start Date*: 2017-07-26 |
| Sponsor Name:Fundación para la Formación e Investigación Sanitarias de la Región de Murcia | ||
| Full Title: PERIPHERAL TRANSCUTANEOUS NEUROMODULATION OF THE POST-TIBIAL NERVE (T-PTNS) FOR SOLIFENACIN 10mg. IN THE TREATMENT OF HYPERACTIVE BLADDER SYNDROME: NON-INFERIORITY PHASE IV RANDOMIZED CLINICAL TRIAL | ||
| Medical condition: Overactive Bladder Syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000307-17 | Sponsor Protocol Number: 69HCL16_0743 | Start Date*: 2018-07-19 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: Microcirculatory and Macrocirculatory Effects of Landiolol on Postoperative Atrial Fibrillation: a Randomized Study. MMELPOAF study. | |||||||||||||
| Medical condition: Postoperative Atrial Fibrillation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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