- Trials with a EudraCT protocol (487)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (22)
487 result(s) found for: Prevalence.
Displaying page 1 of 25.
EudraCT Number: 2019-002762-12 | Sponsor Protocol Number: SJ-674 | Start Date*: 2021-12-07 |
Sponsor Name:Zealand University Hospital | ||
Full Title: The prevalence of bile acid diarrhéa and the effect of budesonid on the bile acid homeostasis in patients with microscopic colitis | ||
Medical condition: Microscopic colitis Bile acid diarrhea | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-005110-58 | Sponsor Protocol Number: 64024 | Start Date*: 2018-06-14 |
Sponsor Name:Medical Centre Leeuwarden | ||
Full Title: Efficacy of a predefined vitamin D dosing regimen in vitamin D-insufficient multiple myeloma patients. | ||
Medical condition: Hypovitaminosis D | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001325-33 | Sponsor Protocol Number: CELLIMIN | Start Date*: 2015-07-02 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Prospective donor-specific Cellular alloresponse assessment for Immunosuppression Minimization in de novo renal transplantation | ||
Medical condition: kidney transplant patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2015-004425-13 | Sponsor Protocol Number: PP01 | Start Date*: 2016-01-22 | |||||||||||
Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
Full Title: Prospective evaluation of 68-Ga-PSMA-PET and early PSA kinetics during salvage radiotherapy for personalizing the management of men with relapse of prostate cancer after radical prostatectomy. | |||||||||||||
Medical condition: Patients with prostate cancer, with a PSA recurrence of ˃ 0.2 ng/ml after prostatectomy, and who are going to receive radiotherapy to the prostate bed. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001071-30 | Sponsor Protocol Number: V1 | Start Date*: 2010-01-21 |
Sponsor Name:Medical University Vienna- Dept. of Pediatric Hemostaselology | ||
Full Title: Aspirin Resistance in Children after Interventional Cardiac Catheterization: The ARC Study | ||
Medical condition: children after interventional cardiac catheterization. | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002880-26 | Sponsor Protocol Number: AI424-128 | Start Date*: 2005-04-06 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: A Phase IV, Multi-center, Cross-sectional study to evaluate the I50L substitution among subjects experiencing virologic failure on a HAART regimen containing atazanavir (ATV) Protocol: version 2.0... | ||
Medical condition: Subjects experiencing virologic failure after a HAART regimen containing ATV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-004167-29 | Sponsor Protocol Number: NA | Start Date*: 2021-03-15 |
Sponsor Name:CHU de Liège | ||
Full Title: Study of the noninferiority of an oral versus intravenous administration of tranexamic acid in total hip arthroplasty | ||
Medical condition: Bleeding in total hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000535-23 | Sponsor Protocol Number: HCB/2021/0060 | Start Date*: 2022-06-20 | |||||||||||
Sponsor Name:Barcelona Institute for Global Health (ISGlobal) | |||||||||||||
Full Title: Efficacy of low dose acetylsalicylic acid in preventing adverse maternal and perinatal outcomes in SARS-CoV-2 infected pregnant women | |||||||||||||
Medical condition: SARS-CoV-2 infection | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001587-29 | Sponsor Protocol Number: 02/04/2020-001 | Start Date*: 2020-04-08 | |||||||||||
Sponsor Name:Barcelona Institute for Global Health (ISGlobal) | |||||||||||||
Full Title: Hydroxychloroquine efficacy in preventing SARS-CoV-2 infection and CoVid-19 disease severity during pregnancy | |||||||||||||
Medical condition: SARS-SoV-2 infection and CoVid-19 disease | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000953-30 | Sponsor Protocol Number: EPAAC | Start Date*: 2019-07-25 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: Effects of phenoximetylpenicillin, amoxicillin and amoxicillin-clavulanic acid on the gut microbiota of healthy volunteers: a randomized clinical trail | ||
Medical condition: Effects of phenoximetylpenicillin, amoxicillin and amoxicillin-clavulanic acid on the gut microbiota of healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004080-70 | Sponsor Protocol Number: | Start Date*: 2011-11-17 |
Sponsor Name:Med. Univ. Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie | ||
Full Title: Preoperative parenteral thiamine supplementation in patients undergoing heart surgery – a pilot study | ||
Medical condition: The objective of this study is to determine the prevalence of thiamine deficiency (TD) in patients with heart surgery, to examine the association between thiamine levels and lactic acidosis and to ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004749-40 | Sponsor Protocol Number: PEDMet 2006-1 | Start Date*: 2006-11-20 |
Sponsor Name:Pediatrics | ||
Full Title: Glucose metabolism in patients with neurological/neuromuscular diseases. | ||
Medical condition: Patients with neurological/neuromuscular diseases | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012300-69 | Sponsor Protocol Number: Number 1 | Start Date*: 2010-03-26 |
Sponsor Name:Meander Medisch Centrum | ||
Full Title: Does vitamin D deficiency contribute to fatigue in patients in remission after treatment of gynaecological malignancy? | ||
Medical condition: Vitamin D deficiency in patients in complete remission after successful treatment of a gynaecological malignancy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000379-14 | Sponsor Protocol Number: APC009 | Start Date*: 2006-04-07 |
Sponsor Name:Alimentary Health Ltd | ||
Full Title: A double-blind randomised placebo controlled feeding study to establish the effect of a probiotic strain on the course of Clostridium difficile carriage in humans. | ||
Medical condition: Clostridium difficile infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000228-33 | Sponsor Protocol Number: CE/17-12-06 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHU Saint-Pierre | |||||||||||||
Full Title: Prospective longitudinal study on immunogenicity, induction of cellular immune responses and safety of vaccination against HPV with the 9valent vaccine in HIV-positive women | |||||||||||||
Medical condition: Immune responses to administration of 9valent vaccine against HPV in HIV-positive women | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021788-33 | Sponsor Protocol Number: A3051075 | Start Date*: 2011-07-13 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 4, MULTI-NATIONAL, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF VARENICLINE COMPARED TO PLACEBO FOR SMOKING CESSATION THROUGH REDUCTION | |||||||||||||
Medical condition: Smoking Cessation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000761-37 | Sponsor Protocol Number: A3051073 | Start Date*: 2018-03-23 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: A Twelve-week, Randomized, Double-blind, Placebo-controlled, Parallel-group, Dose-ranging Study With Follow-up Evaluating The Safety And Efficacy Of Varenicline For Smoking Cessation In Healthy Ado... | |||||||||||||
Medical condition: NICOTINE DEPENDENCE | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002203-15 | Sponsor Protocol Number: PregMet2 | Start Date*: 2012-08-08 | |||||||||||
Sponsor Name:NTNU, Norwegian University of Science and Technology | |||||||||||||
Full Title: Metformin treatment of pregnant PCOS women and prevention of late miscarriages and preterm birth The PregMet 2 Study | |||||||||||||
Medical condition: Poly Cystic Ovarial Syndrome (PCOS) in pregnant women. PCOS should be diagnosed according to the Rotterdam Consensus criterias: - at least 2 out of 3 criterias 1.PCO in at least one ovary 2.Olig... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NO (Completed) SE (Completed) IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000013-20 | Sponsor Protocol Number: 2018-000013-20 | Start Date*: 2018-05-07 |
Sponsor Name:KU Leuven | ||
Full Title: Placebo-controlled crossover study of the ability of Naloxegol to reverse opioid effect on colonic motor patterns in healthy volunteers | ||
Medical condition: This study will be performed in healthy volunteers. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004680-31 | Sponsor Protocol Number: 2018-004680-31 | Start Date*: 2019-08-16 | ||||||||||||||||
Sponsor Name:Lene Ringholm | ||||||||||||||||||
Full Title: A randomised controlled trial comparing the effect of the faster-acting insulin analog - insulin Fiasp® – versus insulin Novorapid® in the treatment of women with type 1 or type 2 diabetes during p... | ||||||||||||||||||
Medical condition: Type 1 and type 2 diabetes during pregnancy and lactation | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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