- Trials with a EudraCT protocol (30)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
30 result(s) found for: Tonsils.
Displaying page 1 of 2.
EudraCT Number: 2013-000492-32 | Sponsor Protocol Number: T16/2013 | Start Date*: 2013-07-10 |
Sponsor Name:Turku University Hospital | ||
Full Title: T cell and interferon expression in tonsils after sublingual immunotherapy and/or nasal live attenuated influenza vaccine | ||
Medical condition: We investigate the effects of allergen and virus on patients with recurrent tonsillitis or tonsillar hypertrphy. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004620-10 | Sponsor Protocol Number: 719-13 | Start Date*: 2014-12-22 |
Sponsor Name:Johan Hellgren | ||
Full Title: A double blind, placebo controlled randomized study of nasal steroid spray treatment on the quality of life and objective sleep parameters in children with sleep disorder breathing. | ||
Medical condition: Sleep disordered breathing due to enlarged tonsils and/or adenoid | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001430-34 | Sponsor Protocol Number: 10-TT-EP-003 | Start Date*: 2012-08-14 | |||||||||||
Sponsor Name:Deutsche Homöopathie-Union, DHU-Arzneimittel GmbH & Co. KG | |||||||||||||
Full Title: Therapeutic effectiveness, safety and tolerability of Tonsilotren tablets in patients (6 to 60 years old) with chronic tonsillitis. A randomized, international, multicenter, controlled clinical t... | |||||||||||||
Medical condition: Chronic tonsillitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003119-50 | Sponsor Protocol Number: HYKSKIPU2011-1 | Start Date*: 2011-08-17 | |||||||||||
Sponsor Name:Vesa Kontinen | |||||||||||||
Full Title: Topical anaesthesia for postoperative pain in adult patients undergoing tonsillectomy | |||||||||||||
Medical condition: Adult patients undergoing tonsillectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005789-38 | Sponsor Protocol Number: HU03/ANE/DEXA | Start Date*: 2006-12-11 | |||||||||||
Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola (H.U.D.E.R.F.) | |||||||||||||
Full Title: Dexaméthasone et Amygdalectomie | |||||||||||||
Medical condition: Children aged from 2 to 8 years old requiring tonsillectomy | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002862-15 | Sponsor Protocol Number: BupivacTons20 | Start Date*: 2021-03-03 |
Sponsor Name:Nordland Hospital. Bodø. Dep of Surgery | ||
Full Title: Can topical anaesthesia with bupivacaine reduce pain after tonsillectomy? | ||
Medical condition: Local pain after tonsillectomy, both at rest and during swallowing. Assessed by self-reporting at 1, 2, 3, 4, 5, 6 hours and 1,2,4 and 6 days after surgery. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003856-19 | Sponsor Protocol Number: CVB2018-2 | Start Date*: 2019-01-09 | |||||||||||
Sponsor Name:Department of Otorhinolaryngology, Head and Neck Surgery and Audiology. Rigshospitalet, University Hospital of Cph, DK | |||||||||||||
Full Title: A Phase I Open Label Study Evaluating the Safety and Feasibility of Allogeneic Mesenchymal stem cells for radiation-induced hyposalivation and xerostomia in previous oropharyngeal patients | |||||||||||||
Medical condition: The trial will include participants with Xerostomia ( International Classification of Diseases-10: DQ 838A) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001259-63 | Sponsor Protocol Number: Pollenvaccine2014-01-15 | Start Date*: 2016-03-09 |
Sponsor Name:Department of Clinical Science, Intervention and Technology, Karolinska Institute | ||
Full Title: Intralymphatic immunotherapy in increasing doses up to 10 000 SQ-U -a human randomized clinical trial | ||
Medical condition: Patients with severe to moderate Allegic rhinitis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014827-21 | Sponsor Protocol Number: RD–5103-009-08 | Start Date*: 2010-09-02 |
Sponsor Name:Derby Hospitals NHS Foundation Trust [...] | ||
Full Title: A single centre double blind randomised controlled trial investigating the use of dexamethasone in the treatment of acute tonsillitis. | ||
Medical condition: Acute bacterial tonsillitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000756-34 | Sponsor Protocol Number: StrepA-negativetonsillitis2019 | Start Date*: 2019-05-29 |
Sponsor Name:Region Jönköping County | ||
Full Title: The SANT - study A randomized controlled clinical trial of Streptococcus group A-negative acute tonsillitis in primary health care - a comparison of phenoxymethylpenicillin and no antibiotic treatm... | ||
Medical condition: J03.0 Pharyngotonsillitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-004188-25 | Sponsor Protocol Number: ASST_FARM_ONCO_P-ACC_2022 | Start Date*: 2023-03-03 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||||||||||||
Full Title: P-ACC Trial - Phase II, single arm, multicenter, open-label study of PARP inhibitors + cisplatin in Recurrent and/or Metastatic Adenoid Cystic Carcinoma | ||||||||||||||||||||||||||||
Medical condition: patients with recurrent and/or Metastatic Adenoid Cystic Carcinoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000048-28 | Sponsor Protocol Number: EC002(Quad1) - C59P1 | Start Date*: 2007-06-22 | ||||||||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | ||||||||||||||||||
Full Title: An open lable, randomised, controlled two centre study to evaluate the mucosal immune response to a quadrivalent meningococcal conjugate vaccine in healthy adults. | ||||||||||||||||||
Medical condition: Prevention of meningococcal infection | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001261-16 | Sponsor Protocol Number: Betapred_vid_tonsillektomi | Start Date*: 2018-10-02 |
Sponsor Name:ÖNH-kliniken Sunderby Sjukhus | ||
Full Title: Betamethasone (Betapred®) as premedication for reducing postoperative vomiting and pain after tonsillectomy – a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Postoperative pain, nausea and vomiting following tonsillectomy in patients with chronic or recurrent tonsillitis. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001611-30 | Sponsor Protocol Number: AJAE1001 | Start Date*: 2006-08-22 |
Sponsor Name:Hammersmith Hospital NHS Trust | ||
Full Title: Clinical trial comparing the effect of Acetaminophen and Ibuprofen on the duration of influenza viral shedding in young children (Pilot study) | ||
Medical condition: Influenza in children [positive rapid diagnostic test (QuickVue influenza test)confirmed by influenza PCR] Infants and young children shed the influenza virus for longer periods than adults, durat... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2021-001425-48 | Sponsor Protocol Number: BLUEBERRY | Start Date*: 2021-07-07 |
Sponsor Name:Division of Anaesthesiology - Department of Acute Medicine - Geneva Children's Hospital, University Hospitals of Geneva | ||
Full Title: Dexamethasone and postoperative bleeding following tonsillectomy in children | ||
Medical condition: Tonsillectomy/tonsillotomy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-001314-17 | Sponsor Protocol Number: ANICK01 | Start Date*: 2007-07-10 | |||||||||||
Sponsor Name:ERASME HOSPITAL | |||||||||||||
Full Title: EVALUATION OF A PROTOCOLE FOR ADENOTONSILLECTOMY IN CHILDREN | |||||||||||||
Medical condition: CHILDREN AGED 2 TO 10 YEAR OF AGE SCHEDULED FOR ADENOTONSILLECTOMY IN A ONE DAY HOSPITAL | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001119-19 | Sponsor Protocol Number: A0661206 | Start Date*: 2016-04-13 | ||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||
Full Title: Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/tonsillitis | ||||||||||||||||||
Medical condition: pharyngitis/tonsillitis | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-004245-29 | Sponsor Protocol Number: 501 | Start Date*: 2008-12-08 | ||||||||||||||||
Sponsor Name:R&D Dept Raigmore Hospital, Inverness | ||||||||||||||||||
Full Title: Single Dose Dexamethasone following Aspiration of a Peri-tonsillar Abscess: A Randomised Placebo-Controlled Trial | ||||||||||||||||||
Medical condition: Peri-tonsillar abscess is a common cause for emergency admission to an ENT ward. In Raigmore there are 2-3 admissions per week with a quinsy. The standard management is needle aspiration under loca... | ||||||||||||||||||
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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: 2008-000066-22 | Sponsor Protocol Number: BAY 43-9006 | Start Date*: 2008-04-30 | ||||||||||||||||
Sponsor Name:Christie Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: A Phase 2 study of Sorafenib (BAY 43-9006) in patients with advanced salivary Adenoid Cystic Carcinoma | ||||||||||||||||||
Medical condition: advanced salivary adenoid cystic carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001927-74 | Sponsor Protocol Number: SysVac01-C60P2 (PA/2008/2883) | Start Date*: 2009-01-16 |
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | ||
Full Title: A PHASE II, OPEN LABEL, RANDOMISED, TWO CENTRE STUDY TO EVALUATE THE IMPORTANCE OF NATURALLY INDUCED IMMUNE REGULATION ON THE MUCOSAL IMMUNE RESPONSE TO MENINGOCOCCAL SEROGROUP B OUTER MEMBRANE VES... | ||
Medical condition: "Healthy volunteers" In this project we will establish whether naturally induced mucosal CD25+ T regulatory activity in adults and adolescents modulates the mucosal immune response to systemic Me... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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