- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (45)
36 result(s) found for: Tonsillectomy.
Displaying page 1 of 2.
EudraCT Number: 2017-001014-28 | Sponsor Protocol Number: studioTRAPPED | Start Date*: 2017-10-20 | ||||||||||||||||
Sponsor Name:AZIENDA PROVINCIALE PER I SERVIZI SANITARI - PROVINCIA AUTONOMA DI TRENTO | ||||||||||||||||||
Full Title: Effects of a reduced dose of tramadol intravenous, in association with paracetamol, in control of Postoperative Pain after tonsillectomy or adenotonsillectomy in Paediatric population:a clinical, c... | ||||||||||||||||||
Medical condition: tonsillectomy or adenotonsillectomy | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003705-13 | Sponsor Protocol Number: DOM | Start Date*: 2010-01-25 | |||||||||||
Sponsor Name:Tuula Manner | |||||||||||||
Full Title: DOM- A comparative study with pre-emptive parenteral oxycodone, morphine and dexamethasone in the treatment of postoperative pain in paediatric patients 4 to 12 years of age. | |||||||||||||
Medical condition: paediartic asa 1-2 patients admitted for tonsillectomy | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2007-001170-92 | Sponsor Protocol Number: 16787 | Start Date*: 2007-09-12 |
Sponsor Name:Erasmus MC | ||
Full Title: Dexamethasone for postoperative pain relief following tonsillectomy in children | ||
Medical condition: (Adeno)Tonsillectomy and Pain | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000202-29 | Sponsor Protocol Number: 2CA_2019_ORL_01 | Start Date*: 2020-07-27 | |||||||||||
Sponsor Name: Centro Clínico Académico - Braga, Associação (2CA-Braga) | |||||||||||||
Full Title: Single-center, double-blind, placebo-controlled study evaluating the efficacy of pre-incisional local analgesia with ropivacaine and dexamethasone for pain management after tonsillectomy | |||||||||||||
Medical condition: Patients selected for tonsillectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007625-43 | Sponsor Protocol Number: 2007PCT018 | Start Date*: 2008-04-18 |
Sponsor Name:Birmingham Children’s Hospital NHS Foundation Trust | ||
Full Title: A randomised controlled trial of two analgesic techniques for the control of pain and post-operative nausea and vomiting in paediatric day-case tonsillectomy. | ||
Medical condition: Tonsillectomy is one of the most common surgical procedures in children and is usually associated with moderate to severe pain which is problematic to treat because of side effects associated with ... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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: 2007-006117-16 | Sponsor Protocol Number: Puranik 07-03/23 | Start Date*: 2008-07-31 |
Sponsor Name:Betsi Cadwaladr University Health Board | ||
Full Title: A prospective, randomised, phase IV, open label clinical trial to study the therapeutic use of buprenorphine 20 mg (BuTrans 20µg/h) matrix transdermal patch in the management of post tonsillectomy ... | ||
Medical condition: post-tonsillectomy pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004274-10 | Sponsor Protocol Number: Etoric-TE-1 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:Freistaat Bayern | |||||||||||||
Full Title: Analgesic efficacy and safety of etoricoxib in ear nose throat surgery | |||||||||||||
Medical condition: The aim of this study is to test the analgesic efficacy and safety of etoricoxib (90 mg or 120 mg qd. perioperatively) for post-operative pain relief in tonsillectomy patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001656-21 | Sponsor Protocol Number: KF0151Y/06 | Start Date*: 2005-08-11 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized, multi-center, double-blind, parallel-group, multiple-dose study assessing the analgesic efficacy and safety of 3 different doses of GRT0151Y compared to placebo and an active comparat... | |||||||||||||
Medical condition: Postoperative pain following tonsillectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) FI (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: 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: 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 |
EudraCT Number: 2022-002496-11 | Sponsor Protocol Number: 07072022v1.0 | Start Date*: 2022-10-03 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: METATONS - Intraoperative methadone for postoperative pain in patients undergoing tonsillectomy - a randomized controlled trial | |||||||||||||
Medical condition: Same-day tonsillectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002213-12 | Sponsor Protocol Number: I10 005 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:CHU de Limoges | ||||||||||||||||||
Full Title: Paracetamol and setrons : drug interactions in the management of pain after tonsillectomy in children | ||||||||||||||||||
Medical condition: Pain | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: View results |
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: 2016-003260-39 | Sponsor Protocol Number: ML16633 | Start Date*: 2016-08-05 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: Intravenous Granisetron (Kytril) in the Prevention of Post-Operative Nausea and Vomiting (PONV) in Pediatric Subjects Undergoing Tonsillectomy or Adenotonsillectomy | |||||||||||||
Medical condition: Prevention of Post-operative Nausea and Vomiting (PONV) in pediatric subjects | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010064-42 | Sponsor Protocol Number: TonsilsTramadolMagnesium TTM1 | Start Date*: 2009-02-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: The effects of peritonsillar infiltration of tramadol versus tramadol plus magnesium on post-tonsillectomy pain | |||||||||||||
Medical condition: Tonsillectomy patients | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001677-81 | Sponsor Protocol Number: PTRS01 | Start Date*: 2019-11-27 |
Sponsor Name:Akershus Universitetssykehus | ||
Full Title: Remifentanil tapering and post-adenotonsillectomy pain in children: a randomised, placebo controlled, double blind study | ||
Medical condition: Tonsillectomy and adenotonsillectomy | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: View results |
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