- Trials with a EudraCT protocol (77)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
77 result(s) found for: Bronchiolitis.
Displaying page 1 of 4.
EudraCT Number: 2013-000499-14 | Sponsor Protocol Number: P120110 | Start Date*: 2013-08-30 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004171-39 | Sponsor Protocol Number: INCB39110-214 | Start Date*: 2020-01-10 | ||||||||||||||||
Sponsor Name:Incyte Corporation | ||||||||||||||||||
Full Title: An Open-Label, Single-Arm, Phase 1/2 Study Evaluating the Safety and Efficacy of Itacitinib in Participants With Bronchiolitis Obliterans Syndrome Following Lung Transplantation | ||||||||||||||||||
Medical condition: Bronchiolitis Obliterans Syndrome following Lung Transplantation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002477-38 | Sponsor Protocol Number: P140929 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022467-36 | Sponsor Protocol Number: IFN_BOSZT_01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Freistaat Bayern | |||||||||||||
Full Title: A phase II study about interferon gamma 1b to therapy the steroid-refractory bronchiolitis obliterans after allogenic stem cell therapy | |||||||||||||
Medical condition: steroid-refractory bronchiolitis obliterans | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012667-34 | Sponsor Protocol Number: BRONCHIOLITIS | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Oslo University Hospital - Ullevål | |||||||||||||
Full Title: BRONCHIOLITIS, OPTIMAL TREATMENT IN INFANTS AND PROGNOSIS | |||||||||||||
Medical condition: Acute bronchiolitis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004304-38 | Sponsor Protocol Number: 12011.203 | Start Date*: 2012-01-06 | |||||||||||
Sponsor Name:PARI Pharma GmbH | |||||||||||||
Full Title: A long-term safety follow-up study of L-CsA therapy for patients who participated in study 12011.201 and volunteered to continue or to cross-over to L-CsA inhalation therapy | |||||||||||||
Medical condition: Prevention of Bronchiolitis Obliterans Syndrome in lung transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) DK (Completed) AT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003801-15 | Sponsor Protocol Number: 12011.202 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:PARIPharma GmbH | |||||||||||||
Full Title: A phase II, randomised, double-blind, placebo controlled, parallel group, dose-finding clinical trial to investigate the efficacy and safety of 10 and 20 mg/day aerosolised liposomal ciclosporin A ... | |||||||||||||
Medical condition: Bronchiolitis Obliterans Syndrome | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014758-14 | Sponsor Protocol Number: 201177 | Start Date*: 2010-05-13 | |||||||||||
Sponsor Name:West Middlesex University Hospital | |||||||||||||
Full Title: Does nebulised hypertonic (3%) saline reduce the duration of hospital admission in infants with bronchiolitis? | |||||||||||||
Medical condition: Viral bronchiolitis (in infants aged under 1yr old) | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022172-30 | Sponsor Protocol Number: FENT-PED-01 | Start Date*: 2010-09-10 | ||||||||||||||||
Sponsor Name:Faculty of pharmacy, University of Ljubljana | ||||||||||||||||||
Full Title: ODNOS MED FARMAKOKINETIKO IN FARMAKODINAMIKO FENTANILA PRI OTROCIH (Pharmacokinetics and pharmcodynamics of fentanyl in pediatric population) | ||||||||||||||||||
Medical condition: Children aged less than 2 years that are hospitalized due to bronchiolitis and need sedation and analgesia with fentanyl. | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003800-73 | Sponsor Protocol Number: 12011-201 | Start Date*: 2009-07-14 | |||||||||||
Sponsor Name:PARI Pharma GmbH | |||||||||||||
Full Title: A phase II, multicentre, randomised, double-blind, placebo controlled clinical trial to investigate the efficacy and safety of 10 or 20 mg/day aerosolised liposomal ciclosporin A (L-CsA) versus aer... | |||||||||||||
Medical condition: Prevention of bronchiolitis obliterans syndrome in lung transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) AT (Prematurely Ended) DK (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016925-32 | Sponsor Protocol Number: HSJD-CAFEINA-09 | Start Date*: 2010-03-09 | ||||||||||||||||
Sponsor Name:Hospital Sant Joan de Déu | ||||||||||||||||||
Full Title: "CAFEÍNA COMO TRATAMIENTO DE LAS APNEAS EN PACIENTES CON BRONQUIOLITIS AGUDA" | ||||||||||||||||||
Medical condition: TRATAMIENTO DE LAS APNEAS EN PACIENTES CON BRONQUIOLITIS AGUDA | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002987-29 | Sponsor Protocol Number: BT–L-CsA–303–FU | Start Date*: 2020-02-12 | |||||||||||
Sponsor Name:Zambon SpA | |||||||||||||
Full Title: An Open Label Follow-Up Study to Evaluate the Long Term Safety and Efficacy of L-CSA in Patients with a Diagnosis of CLAD-BOS after they have completed the participation to BOSTON 1 and BOSTON 2 st... | |||||||||||||
Medical condition: Bronchiolitis Obliterans Syndrome in Patients post Single or post Double Lung Transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) ES (Ongoing) AT (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003007-36 | Sponsor Protocol Number: HP002A | Start Date*: 2006-08-02 | |||||||||||
Sponsor Name:Imperial College London [...] | |||||||||||||
Full Title: B.R.E.A.T.H.E. Bronchiolitis RCT: Emergency Assisted Therapy with Heliox - an Evaluation. A Prospective, Double-Blinded, Randomised, Controlled Clinical Trial to assess the effect of helium-oxygen ... | |||||||||||||
Medical condition: Bronchiolitis | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003893-46 | Sponsor Protocol Number: NA | Start Date*: 2009-11-03 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:KULeuven and University Hospitals Leuven (Leuven Lung Transplant Group) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: AZITHROMYCIN IN BRONCHIOLITIS OBLITERANS SYNDROME | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: - Chronic rejection at 1 and 2 year post-lung transplantation - Mortality at 1 and 2 year post-lung transplantation - Acute rejection rate at 1 and 2 post-lung transplantation - Infection rate at 1... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021983-14 | Sponsor Protocol Number: MLK002 | Start Date*: 2010-09-23 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:UZ Gasthuisberg | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized placebo-controlled double blind study to treat BOS. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: -Mortality at 1 and 2 year post diagnosis of BOS -Infection rate during BOS -Evolution of pulmonary function after diagnosis of BOS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022027-30 | Sponsor Protocol Number: VIT001 | Start Date*: 2010-09-23 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:UZ Gasthuisberg | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomized placebo-controlled double blind study to prevent BOS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: A study to prevent the occurence of chronic rejection after lung transplantation. Other points of investigation include lung function evolution, rate of survival, BAL cellularity, infection rate, r... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003093-32 | Sponsor Protocol Number: RC25/13 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:IRCCS Burlo Garofolo | |||||||||||||
Full Title: Randomized controlled trial to evaluate the efficacy of high flow versus low flow oxygen therapy in bronchiolitis | |||||||||||||
Medical condition: Bronchiolitis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001768-39 | Sponsor Protocol Number: SURFABRON | Start Date*: 2018-03-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA INTEGRATA VERONA | |||||||||||||
Full Title: Randomized multicentre-controlled, placebo-controlled (1: 1) study to evaluate the efficacy and safety of Curosurf in patients under 12 months of age with moderate or severe acute respiratory distr... | |||||||||||||
Medical condition: Acute severe hypoxic bronchiolitis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024230-35 | Sponsor Protocol Number: EMABRHIP | Start Date*: 2012-04-25 | |||||||||||
Sponsor Name:Fundacion par la investigación biomédica del Hospital Universitario La Paz | |||||||||||||
Full Title: Effectiveness of hipertonic saline serum 3% nebulized in bronchiolitis | |||||||||||||
Medical condition: Bronchiolitis | |||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002980-25 | Sponsor Protocol Number: PRESERV | Start Date*: 2020-06-12 | |||||||||||
Sponsor Name:OSP.DEGLI INFERMI DI BIELLA | |||||||||||||
Full Title: Randomized, multicenter, open-label study on PREvention of respiratory SEquelae of RSV bronchiolitis in preterm babies (PRESERV) | |||||||||||||
Medical condition: Respiratory sincizial virus (RSV) bronchiolitis | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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