- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
85 result(s) found for: Colony forming units.
Displaying page 2 of 5.
EudraCT Number: 2011-002343-99 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-01-03 |
Sponsor Name:Heart of England NHS Foundation Trust | ||
Full Title: An Open-label Study into the Efficacy and Dosing of Probiotic Escherichia coli Nissle 1917 for Prevention of Gram-negative Gastric Colonisation in Ventilated Intensive Care Patients. | ||
Medical condition: Gastric colonisation by pathogenic gram negative bacteria in ventilated adult ICU patients and it's prevention by the probiotic E.coli Nissle 1917 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000342-22 | Sponsor Protocol Number: VALACT-2017-01 | Start Date*: 2017-04-04 | |||||||||||
Sponsor Name:Dr. Luis Fernández-Dr. Jesus Barrio | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study of the usefulness of the probiotic 'Lactobacillus reuteri' in the therapy of quadruple eradication of Helicobacter pylori infection in usual cli... | |||||||||||||
Medical condition: Helicobacter Pylori infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004811-22 | Sponsor Protocol Number: ABR 14357 | Start Date*: 2008-04-01 | |||||||||||
Sponsor Name:Erasmus Medical Center Rotterdam | |||||||||||||
Full Title: A prospective, randomized, double-blind comparison of 5 % against 1 % povidone-iodine solution in preoperative antisepsis for strabismus surgery in young children. | |||||||||||||
Medical condition: Endophthalmitis (E) after strabismus surgery (S) leading to blindness is caused by eyelid and conjunctival bacteria. Povidone-iodine(PI) solutions between 1% and 5% reduce the number of bacteria on... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009869-34 | Sponsor Protocol Number: BAYq3939/12965 | Start Date*: 2009-06-08 | ||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||
Full Title: Randomized, placebo-controlled, double-blind, multi center study to evaluate the safety and efficacy of ciprofloxacin inhale compared to placebo in patients with non-cystic fibrosis bronchiectasis | ||||||||||||||||||
Medical condition: Idiopathic and post-pneumonic non-Cystic Fibrosis Bronchiectasis in pulmonary stable patients (defined as FEV1 of > 35 % and < 80 percent of predicted) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000395-97 | Sponsor Protocol Number: GS-US-205-0117 | Start Date*: 2015-02-02 |
Sponsor Name:Gilead Sciences, Inc. [...] | ||
Full Title: A Double-Blind, Multicenter, Multinational, Randomized, Placebo-Controlled Trial Evaluating Aztreonam Lysine for Inhalation in Patients with Cystic Fibrosis, Mild Lung Disease, and P. aeruginosa (A... | ||
Medical condition: Cystic Fibrosis with Mild Lung Disease and P. aeruginosa (AIR-CF4) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-003700-36 | Sponsor Protocol Number: TCI 0107 | Start Date*: 2008-06-09 |
Sponsor Name:Unidad de Trasplantes y Terapia Celular del Hospital General Universitario Central de Asturias | ||
Full Title: Estudio abierto con evaluador ciego de la eficacia de las células mononucleares autólogas de médula ósea en la regeneración celular de un paciente con ictus isquémico agudo de la ACM | ||
Medical condition: TRATAMIENTO CON CÉLULAS MADRE DE MÉDULA OSEA EN PACIENTES CON ICTUS ISQUÉMICO AGUDO | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000944-13 | Sponsor Protocol Number: GEN-004-002 | Start Date*: 2014-07-30 | |||||||||||
Sponsor Name:Genocea Biosciences, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of GEN-004, a Pneumococcal Protein Subunit Vaccine, on Colonization Following Intran... | |||||||||||||
Medical condition: Pneumococcal Nasal Carriage | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002438-38 | Sponsor Protocol Number: HT-09 | Start Date*: 2012-02-21 | |||||||||||
Sponsor Name:Helperby Therapeutics Limited | |||||||||||||
Full Title: An open-label, multiple dose, efficacy study of HT61 in combination with marketed antibiotics, applied to the anterior nares in subjects with nasal carriage of Staphylococcus aureus (S. aureus). | |||||||||||||
Medical condition: Nasal carriage of Staphylococcus aureus (including MRSA) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004046-41 | Sponsor Protocol Number: 273551 | Start Date*: 2021-12-09 |
Sponsor Name:University of Bergen, | ||
Full Title: A multicentre clinical trial; Alveolar bone augmentation using Mesenchymal Stem Cells and biphasic calcium phosphate granules prior to dental implants | ||
Medical condition: Patients in need of dental implant(s) in the upper and lower jaws with presence of bone defects with loss in vertical height and < than 4 mm in lateral width | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003756-11 | Sponsor Protocol Number: MU0728 | Start Date*: 2008-06-17 | |||||||||||
Sponsor Name:Ardeypharm GmbH | |||||||||||||
Full Title: Behandlung der Darm-assoziierten Halitosis mit E. coli Stamm Nissle 1917 Treatment for GUT-Caused Halitosis With with E. coli strain Nissle 1917 | |||||||||||||
Medical condition: gut-caused halitosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002871-24 | Sponsor Protocol Number: AG019-T1D-101 | Start Date*: 2018-10-15 | |||||||||||
Sponsor Name:Intrexon T1D Partners, LLC (IT1D) | |||||||||||||
Full Title: A prospective, multi-center, Phase 1b/2a study to assess the safety and tolerability of different doses of AG019 administered alone or in association with teplizumab in patients with clinical recen... | |||||||||||||
Medical condition: Recent-onset Type 1 Diabetes mellitus (T1D) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019254-40 | Sponsor Protocol Number: C10-109-02 | Start Date*: 2010-11-02 | |||||||||||
Sponsor Name:Lytix Biopharma AS | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, ascending dose Phase I/IIa study to evaluate the safety, tolerability and efficacy of topical LTX-109 in subjects nasally colonized with methicillin-... | |||||||||||||
Medical condition: Nasal decolonization of MRSA/MSSA | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002507-28 | Sponsor Protocol Number: OPHT-280515 | Start Date*: 2015-07-20 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Effect of benzalkonium chloride containing eye drops on the conjunctival bacterial flora of dry eye patients. | |||||||||||||
Medical condition: conjunctival bacterial flora in patients with dry eye syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004653-25 | Sponsor Protocol Number: Repha_1362 | Start Date*: 2014-05-02 | ||||||||||||||||
Sponsor Name:Repha GmbH | ||||||||||||||||||
Full Title: Clinical trial for examination of efficacy and safety of ANGOCIN® Anti-Infekt N versus placebo in the continous prophylaxis of chronically recurring uncomplicated cystitis | ||||||||||||||||||
Medical condition: Continuous prophylaxis of chronically recurring uncomplicated cystitis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001678-31 | Sponsor Protocol Number: APHP200462 | Start Date*: 2020-04-28 |
Sponsor Name:Assistance Publique Hopitaux de Paris | ||
Full Title: Randomized controlled trial evaluating the efficacy of vaccination with Bacillus Calmette and Guérin (BCG) in the Prevention of COVID-19 via the strengthening of innate immunity in Health Care Work... | ||
Medical condition: COVID 19 Health care workers (medical or non-medical) in French hospitals in direct contact with COVID-19 patients, including nurses, medical doctors and other personnel working in wards in charge... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001398-34 | Sponsor Protocol Number: BMMNC_PTA_001 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:Institut klinické a experimentální medicíny | |||||||||||||
Full Title: A prospective, randomized study to assess the effect of autologous bone marrow-derived mononuclear cell therapy and its combination with percutaneous transluminal angioplasty (PTA) in comparison wi... | |||||||||||||
Medical condition: In our study, the effect of autologous cell therapy (ACT) will be compared with repeated percutaneous transluminal angioplasty (re-PTA) in patients with diabetic foot and then will be compared the ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001397-15 | Sponsor Protocol Number: BMMNC_CLI_001 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:Institut klinické a experimentální medicíny | |||||||||||||
Full Title: A prospective, randomized study to compare the effect on tissue oxygenation and clinical outcome of autologous bone marrow-derived mononuclear cell therapy with standard treatment in patients with ... | |||||||||||||
Medical condition: Autologous cell therapy (ACT) is new technique for patients with critical limb ischemia and diabetic foot (DF). In our study, the effect of ACT and also the repetitive treatment will be compared wi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004402-10 | Sponsor Protocol Number: APHP180587 | Start Date*: 2020-03-11 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Fecal transplantation to Eradicate Colonizing Emergent Superbugs | |||||||||||||
Medical condition: Patients colonized with MDR-GNB (multi-drug resistant Gram Negative bacteria ) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006228-36 | Sponsor Protocol Number: LT1225-PII-03/06 | Start Date*: 2008-01-24 | |||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||
Full Title: Evaluación de la Eficacia y Seguridad de Azyter® (T1225) en la Profilaxis Antibiótica Perioperatoria (descontaminación de la superficie ocular) para la Cirugía de Catarata | |||||||||||||
Medical condition: Profilaxis Antibiótica Perioperatoria (descontaminación de la superficie ocular) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001565-33 | Sponsor Protocol Number: CTBM100C2403 | Start Date*: 2013-06-21 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: An open-label, crossover, interventional Phase IV study to compare the ease of use of tobramycin inhalation powder with tobramycin inhalation solution and nebulized colistimethate for the treatment... | ||||||||||||||||||
Medical condition: Chronic lung infection with Pseudomonas aeruginosa in cystic fibrosis patients | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) IE (Completed) | ||||||||||||||||||
Trial results: View results |
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