- Trials with a EudraCT protocol (35)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
35 result(s) found for: Chronic sinusitis.
Displaying page 1 of 2.
| 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | ||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||||||||||||||||||||||
| 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. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| 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 | ||||||||||||||||||
|
||||||||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||||||||||||
| 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) | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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 | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
| 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 | |||||||||||||
|
|||||||||||||
| 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: 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 | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001803-35 | Sponsor Protocol Number: ACT12340 | Start Date*: 2013-07-31 | |||||||||||
| Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
| Full Title: A Randomized, Double-Blind, Phase 2, Placebo Controlled, 2 Arm Study To Evaluate Dupilumab In Patients With Bilateral Nasal Polyposis And Chronic Symptoms Of Sinusitis | |||||||||||||
| Medical condition: Nasal polyps | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) SE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004437-18 | Sponsor Protocol Number: 2343453 | Start Date*: 2006-07-18 |
| Sponsor Name:Department of Otolaryngology, Head and Neck Surgery Johannes Gutenberg-Universität Mainz | ||
| Full Title: Placebo-controlled double-blind study about the effectiveness of longtime acetylsalicylic acid desactivation therapy as prevention of recurrens of poyposis nasi in case of acetylsalicylic acid int... | ||
| Medical condition: chronic rhinosinusistis, polyposis nasi, aspirin intolerance | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-000585-15 | Sponsor Protocol Number: CBP-201-WW003 | Start Date*: 2021-11-11 | |||||||||||
| Sponsor Name:Suzhou Connect Biopharmaceuticals Ltd. | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate CBP-201 in Adult Patients with Chronic Rhinosinusitis with Nasal Polyps | |||||||||||||
| Medical condition: Chronic Rhinosinusitis with Nasal Polyps | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012505-18 | Sponsor Protocol Number: nexiam2009 | Start Date*: 2009-07-02 | ||||||||||||||||
| Sponsor Name:UZLeuven [...] | ||||||||||||||||||
| Full Title: A randomized double-blind placebo controlled trial evaluating the effect of esomeprazole (nexiam) 40 mg twice daily in subjects with chronic unexplained cough | ||||||||||||||||||
| Medical condition: gastroesophageal reflux and chronic cough | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-004734-37 | Sponsor Protocol Number: NORM-01 | Start Date*: 2021-12-14 | |||||||||||
| Sponsor Name:Octapharma Pharmazeutika Prod.Ges.m.b.H | |||||||||||||
| Full Title: Prospective, open-label, single-arm, multicentre Phase 3 study to evaluate the pharmacokinetics, efficacy, tolerability, and safety of subcutaneous human immunoglobulin (Newnorm) in patients with p... | |||||||||||||
| Medical condition: Primary Immunodeficiency Diseases | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) SK (Trial now transitioned) PL (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.