- Trials with a EudraCT protocol (325)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
325 result(s) found for: Leukocyte.
Displaying page 1 of 17.
EudraCT Number: 2013-001948-60 | Sponsor Protocol Number: DOSFEM | Start Date*: 2013-09-09 |
Sponsor Name:Sint Franciscus Gasthuis Rotterdam | ||
Full Title: Effects of high and low dose vitamin D on postprandial leukocyte activation, oxidative stress and vascular function in healthy overweight and obese females | ||
Medical condition: 'healthy volunteers' 'atherosclerosis' 'vitamin D deficiency' | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001080-24 | Sponsor Protocol Number: NL76906.068.21 | Start Date*: 2021-04-08 |
Sponsor Name:Maastricht University | ||
Full Title: The effect of plant stanol ester consumption on the vaccination response to a COVID-19 vaccine | ||
Medical condition: COVID-19 vaccination respons of people with BMI 27-35 kg/m2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-001417-24 | Sponsor Protocol Number: PLEIADES | Start Date*: 2017-02-22 |
Sponsor Name:Franciscus Gasthuis | ||
Full Title: POSTPRANDIAL LIPEMIA, INFLAMMATION, AND VASCULAR FUNCTION IN DIABETES MODULATED BY SGLT2 INHIBITION | ||
Medical condition: Diabetes Mellitus type II | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005553-39 | Sponsor Protocol Number: 1501 | Start Date*: 2015-12-29 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Effects of Sativex on blood leukocytes in patients with lymphoma/chronic lymphocytic leukaemia | ||
Medical condition: Lymphoma and chronic lymphocytic leukaemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003601-10 | Sponsor Protocol Number: NL69300 | Start Date*: 2020-09-18 | |||||||||||
Sponsor Name:Amsterdam University Medical Centers | |||||||||||||
Full Title: Treatment of Skin Severity in Ichthyosis with Hyperbaric Oxygen Therapy | |||||||||||||
Medical condition: ichthyosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003041-14 | Sponsor Protocol Number: 565 | Start Date*: 2005-09-20 |
Sponsor Name:Department of Clinical Pharmacology, Medical University of Vienna | ||
Full Title: Anti-inflammatory effect of statins in the human endotoxin model | ||
Medical condition: Healthy volunteers are tested in an endotoxemia model | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003253-15 | Sponsor Protocol Number: 58836 | Start Date*: 2017-01-25 |
Sponsor Name:Franciscus Gasthui | ||
Full Title: MODULATION OF POSTPRANDIAL LIPEMIA, INFLAMMATION, AND VASCULAR FUNCTION BY PCSK9 INHIBITION IN DIABETES. | ||
Medical condition: Diabetes mellitus type 2 | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004792-14 | Sponsor Protocol Number: 0298-21 | Start Date*: 2021-09-08 | |||||||||||
Sponsor Name:Intas Pharmaceuticals Ltd. | |||||||||||||
Full Title: A Randomized, Active-Controlled, Multicenter, Open label, Two Arm Study to Assess Safety, Efficacy, Pharmacodynamics, and Pharmacokinetics with Pegfilgrastim PFS of Intas Pharmaceutical Limited Com... | |||||||||||||
Medical condition: Paediatric Patients Under 6 years of Age with Rhabdomyosarcoma or Wilms’ Tumour on Myelosuppressive Chemotherapy (CmT) Regimen | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000517-33 | Sponsor Protocol Number: RP-L201-0318 | Start Date*: 2020-07-14 | |||||||||||
Sponsor Name:Rocket Pharmaceuticals, Inc. | |||||||||||||
Full Title: Gene Therapy for Leukocyte Adhesion Deficiency-I (LAD-I):A Phase I/II Clinical Trial to Evaluate the Safety and Efficacy of the Infusion of Autologous Hematopoietic Stem Cells Transduced with a Len... | |||||||||||||
Medical condition: Leukocyte Adhesion Deficiency-I (LAD-I) | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002680-26 | Sponsor Protocol Number: RP-L201-0218 | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:Rocket Pharmaceuticals, Inc. | |||||||||||||
Full Title: Gene Therapy for Leukocyte Adhesion Deficiency-I (LAD-I): A Phase I Clinical Trial to Evaluate the Safety and Efficacy of the Infusion of Autologous Hematopoietic Stem Cells Transduced with a Lenti... | |||||||||||||
Medical condition: Leukocyte Adhesion Deficiency-I (LAD-I) | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005687-97 | Sponsor Protocol Number: NoSIRS | Start Date*: 2013-06-20 |
Sponsor Name:Medtronic Inc. | ||
Full Title: Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a pilot study | ||
Medical condition: Possible future indications: inflammatory conditions in general | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004137-21 | Sponsor Protocol Number: 78591.041.21 | Start Date*: 2021-10-28 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Effect of intranasal administration of palivizumab on experimental respiratory syncytial viral infection – a human challenge study | ||
Medical condition: respiratory syncytial virus infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002497-27 | Sponsor Protocol Number: KFJ-2020-01_IMUNOR | Start Date*: 2020-10-27 |
Sponsor Name:Thomayerova nemocnice | ||
Full Title: A randomized, open-label, phase IV monocentric study evaluating the clinical effect of oral immunomodulatory therapy with IMUNOR® in patients with moderate COVID-19 disease | ||
Medical condition: Patients with COVID -19 disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004682-39 | Sponsor Protocol Number: KFJ-2020-02_NORMOSANG | Start Date*: 2020-11-16 |
Sponsor Name:Thomayerova nemocnice | ||
Full Title: Pilot, open-label, monocentric study evaluating safety and clinical effect of application of NORMOSANG® in patients with COVID-19 disease | ||
Medical condition: Patients with COVID -19 disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005374-26 | Sponsor Protocol Number: ECAELEV21 | Start Date*: 2022-08-18 |
Sponsor Name:OMEQUI coordinator | ||
Full Title: Efficacy of platelet- and leukocyte-rich fibrin (L-PRF) in reducing healing time in sinus lift combined with deproteinized bovine mineralized bone (DBBM): randomized clinical trial. | ||
Medical condition: If the application of L-PRF with respect to the use of DBBM shows that there are differences in the percentage of new bone between the LPRF group and the control group at 4 and 6 months | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004135-77 | Sponsor Protocol Number: 68010 | Start Date*: 2019-04-03 |
Sponsor Name:MUMC | ||
Full Title: Randomized controlled trial on the effect of vitamin C supplementation in autologous stem cell transplantations | ||
Medical condition: adults (minimally 18 years old) that are planed to receive an autologous stem cell transplantation for a hematological malignancy (myeloma or lymphoma) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002052-84 | Sponsor Protocol Number: STX-01 | Start Date*: 2014-07-24 | |||||||||||
Sponsor Name:STX Pharma | |||||||||||||
Full Title: An Exploratory Phase IIa Study to Investigate the Biological Activity of Oral FX125L in Adult Patients with Mild to Moderate Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2013-001178-20 | Sponsor Protocol Number: IM103-307,SMR-2729 | Start Date*: 2013-10-29 | |||||||||||
Sponsor Name:Uppsala University Hospital, MHT, Department of Nephrology | |||||||||||||
Full Title: Cardiovascular (CV) risk prediction and CV biomarkers in renal transplant recipients treated with belatacept compared to calcineurin inhibitors (CNI). Open randomized 12 month study. | |||||||||||||
Medical condition: Prophylaxis of graft rejection in adults who have received a renal transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003067-22 | Sponsor Protocol Number: PRISTINE | Start Date*: 2012-11-19 | |||||||||||
Sponsor Name:LUMC | |||||||||||||
Full Title: Pneumonia treated with rifampicine attenuates inflammation | |||||||||||||
Medical condition: Community acquired pneumonia CURB-65 class >1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000839-21 | Sponsor Protocol Number: DREPADOL | Start Date*: 2019-06-17 | |||||||||||
Sponsor Name:Centre Hospitalier Intercommunal de Créteil | |||||||||||||
Full Title: Evaluation of the efficacy and safety of aprepitant in the management of vaso-occlusive crisis in sickle cell children: randomized, single-center, randomized, phase IIb/III prospective study | |||||||||||||
Medical condition: vaso-occlusive crisis for patients with sickle cell disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Not Authorised) | |||||||||||||
Trial results: (No results available) |
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