- Trials with a EudraCT protocol (78)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (37)
78 result(s) found for: Sinusitis.
Displaying page 1 of 4.
| EudraCT Number: 2010-022188-37 | Sponsor Protocol Number: 29072010 | Start Date*: 2010-11-29 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Pirkanmaan sairaanhoitopiiri | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A comparative study between the Relieva Stratus MicroFlow Spacer drug eluting ethmoid sinus stent therapy and the intranasal corticoid steroid therapy in the treatment of patients with chronic rhin... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Kaikki tutkittavat henkilöt niin lääkeimplantti- kuin nenäsumuteverrokkiryhmässä sairastavat kroonista sinuiittia | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2018-001100-11 | Sponsor Protocol Number: 14/0644 | Start Date*: 2018-07-13 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University College London | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Defining best Management in Adult Chronic RhinOsinusitis | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Chronic rhinosinusitis | ||||||||||||||||||||||||||||||||||||||||||||||||
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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: 2007-003739-22 | Sponsor Protocol Number: GAL-01-2007 | Start Date*: 2007-10-04 | |||||||||||
| Sponsor Name:GALSOR S.R.L. | |||||||||||||
| Full Title: Safety and efficacy (for the symptom remission) of the treatment adjuvant of the antibiotic therapy of the acute episode of sinusitis (acute, subacute, chronic)with Ecballium Elaterium (SINUclean D... | |||||||||||||
| Medical condition: Acute sinusitis or exacerbation of subacute or chronic sinusitis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005828-84 | Sponsor Protocol Number: ECP | Start Date*: 2009-04-02 | |||||||||||
| Sponsor Name:ENT Hospital, Johannes-Gutenberg University, Mainz | |||||||||||||
| Full Title: Inflammatory mediators in nasal discharge of chronic rhinosinusitis patients treated with erythromycin. | |||||||||||||
| Medical condition: Effect of erythromycin therapy on the inflammatory mediators in nasal discharge of chronic rhinosinusitis patients. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002779-34 | Sponsor Protocol Number: BAY 12-8039/11881 | Start Date*: 2005-12-13 | |||||||||||
| Sponsor Name:BAYER | |||||||||||||
| Full Title: Prospective, multicenter, randomized, double blind, parallel arm study to evaluate the efficacy and safety of Moxifloxacin 400 mg OD for 7 days versus amoxicillin clavulanate/claritromycin for 10 d... | |||||||||||||
| Medical condition: Acute bacterial rhinosinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001227-13 | Sponsor Protocol Number: SOPAZITHRO | Start Date*: 2022-02-22 | ||||||||||||||||
| Sponsor Name:Centre hospitalier intercommunal de Créteil | ||||||||||||||||||
| Full Title: Evaluation of the Efficacy of 3-month Continuous Extended Treatment With Azithromycin in Idiopathic Purulent Oedematous Sinusitis in Adults: a Multicentre Randomised Controlled Trial | ||||||||||||||||||
| Medical condition: Patients with Purulent Oedematous Sinusitis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2004-001460-42 | Sponsor Protocol Number: HMR 3647A/4023 | Start Date*: 2004-11-16 | |||||||||||
| Sponsor Name:Aventis Intercontinental - Sanofi-aventis | |||||||||||||
| Full Title: A prospective, randomized, open-label, active-controlled study in adult subjects with acute bacterial sinusitis comparing the clinical efficacy of telithromycin (KETEK®) 800 mg once a day for 5 da... | |||||||||||||
| Medical condition: acute bacterial sinusitis (ABS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-002102-37 | Sponsor Protocol Number: ORL-CENS-2015 | Start Date*: 2015-10-02 | ||||||||||||||||
| Sponsor Name:Fundació Parc Taulí | ||||||||||||||||||
| Full Title: Open randomized clinical trial to compare the efficacy of hypotensive anesthesia with clonidine or dexmedetomidine during endoscopic nasal surgery | ||||||||||||||||||
| Medical condition: Nasosinusal endoscopic surgery in patients with chronic sinusitis and/or nasal polyposis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-006911-27 | Sponsor Protocol Number: LYR-210-2021-005 | Start Date*: 2022-07-28 | |||||||||||
| Sponsor Name:Lyra Therapeutics, Inc. | |||||||||||||
| Full Title: ENLIGHTEN 2: A Phase III, Randomized, Blinded, Controlled, Parallel-Group Trial to Evaluate the Efficacy and Safety of LYR-210 for the Treatment of Chronic Rhinosinusitis (CRS) in Adults | |||||||||||||
| Medical condition: Chronic Rhinosinusitis (CRS) in Adults | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Trial now transitioned) DE (Trial now transitioned) BG (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005906-83 | Sponsor Protocol Number: LYR-210-2021-004 | Start Date*: 2022-08-05 | |||||||||||
| Sponsor Name:Lyra Therapeutics, Inc. | |||||||||||||
| Full Title: ENLIGHTEN 1: A Phase III, Randomized, Blinded, Controlled, Parallel-Group Trial to Evaluate the Efficacy and Safety of LYR-210 for the Treatment of Chronic Rhinosinusitis (CRS) in Adults | |||||||||||||
| Medical condition: Chronic Rhinosinusitis (CRS) in Adults | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) PL (Completed) ES (Ongoing) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004621-89 | Sponsor Protocol Number: LYR-210-2018-002 | Start Date*: 2019-07-29 | |||||||||||
| Sponsor Name:Lyra Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase II, Randomized, Blinded, Sham Procedure-Controlled, Parallel-Group Trial to Evaluate the Efficacy, Safety and Tolerability of LYR-210 in Adult Subjects with Chronic Sinusitis (LANTERN Study) | |||||||||||||
| Medical condition: Chronic sinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001435-63 | Sponsor Protocol Number: NACFL-ZI-L-01-06 | Start Date*: 2008-01-28 | |||||||||||
| Sponsor Name:ZAMBON ITALIA | |||||||||||||
| Full Title: AEROSOLIC TREATMENT OF ACUTE AND RECURRENT RHINOSINUSITIS DURING INTERCRITICAL STAGES : SINGLE BLIND CLINICAL STUDY, N-ACETYLCISTEIN VS AMBROXOL, ASSOCIATED WITH CORTISONE THERAPY | |||||||||||||
| Medical condition: Patients with acute recurrent rhinosinusitis(intercritical stages) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005965-18 | Sponsor Protocol Number: ORL-CENS-2012 | Start Date*: 2012-02-21 | ||||||||||||||||||||||||||
| Sponsor Name:Fundació Parc Taulí | ||||||||||||||||||||||||||||
| Full Title: Open randomized trial to compare the bleeding during endoscopic nasal surgery after hypotensive anesthesia with clonidine or remifentanil. | ||||||||||||||||||||||||||||
| Medical condition: Nasosinusal endoscopic surgery in patients with chronic sinusitis and/or nasal polyposis | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-003117-35 | Sponsor Protocol Number: EFC16723 | Start Date*: 2021-03-17 | |||||||||||
| Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, 2-part study to evaluate the efficacy and safety of dupilumab in patients with uncontrolled, chronic rhinosinusitis without nasal polyposis (CRSsNP) | |||||||||||||
| Medical condition: Chronic rhinosinusitis without nasal polyposis | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) PT (Completed) SE (Completed) HU (Completed) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006220-19 | Sponsor Protocol Number: SUM-2006/01-INT | Start Date*: 2008-11-27 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:PLIVA Hrvatska d.o.o. | ||||||||||||||||||||||||||||||||||||||
| Full Title: Safety and Efficacy of Sumamed® Therapy in the Treatment of Respiratory Tract Infections in Adults and Children: International, Multicenter, Non-Comparative Study | ||||||||||||||||||||||||||||||||||||||
| Medical condition: acute pharyngitis/tonsilitis acute sinusitis acute otitis media acute exacerbation of chronic bronchitis community acquired pneumonia | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: SI (Completed) CZ (Ongoing) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-000648-86 | Sponsor Protocol Number: OPN-FLU-CS-3206 | Start Date*: 2019-10-01 | |||||||||||
| Sponsor Name:OptiNose US, Inc. | |||||||||||||
| Full Title: A 24-Week Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study Evaluating the Efficacy and Safety of Intranasal Administration of 186 and 372 μg of OPN-375 Twice a Day (B... | |||||||||||||
| Medical condition: Chronic rhinosinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) PL (Completed) ES (Ongoing) BG (Completed) RO (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000639-13 | Sponsor Protocol Number: A0661142 | Start Date*: 2005-10-10 | |||||||||||
| Sponsor Name:Pfizer Ltd | |||||||||||||
| Full Title: An open-label, multi-center trial of azithromycin pharmacokinetics in sinus aspirate and serum following oral administration of either a 500 mg immediate-release (IR) once-daily 3 day regimen or a ... | |||||||||||||
| Medical condition: Acute bacterial sinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) SE (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000368-12 | Sponsor Protocol Number: OPN-FLU-CS-3205 | Start Date*: 2019-10-01 | |||||||||||
| Sponsor Name:OptiNose US, Inc. | |||||||||||||
| Full Title: A 24-Week Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study Evaluating the Efficacy and Safety of Intranasal Administration of 186 and 372 μg of OPN-375 Twice a Day (... | |||||||||||||
| Medical condition: Chronic sinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005654-53 | Sponsor Protocol Number: BroSin 05 | Start Date*: 2006-12-07 |
| Sponsor Name:Ursapharm Arzneimittel GmbH & Co. KG | ||
| Full Title: "Explorative triple-arm dosis-finding study for examination about the effectivity and tolerance of Bromelain by acute sinusitis" | ||
| Medical condition: Therapy of acute sinusitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001837-16 | Sponsor Protocol Number: 027SC05134 | Start Date*: 2006-05-16 | |||||||||||
| Sponsor Name:ANGELINI | |||||||||||||
| Full Title: PRULIFLOXACIN VERSUS LEVOFLOXACIN IN PATIENTS WITH ACUTE BACTERIAL RHINOSINUSITIS ABRS | |||||||||||||
| Medical condition: ACUTE BACTERIAL RHINOSINUSITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) HU (Completed) AT (Completed) ES (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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