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Clinical trials for Triamcinolone hexacetonide

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

    • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).

    The EU Clinical Trials Register currently displays   44334   clinical trials with a EudraCT protocol, of which   7366   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
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    7 result(s) found for: Triamcinolone hexacetonide. Displaying page 1 of 1.
    EudraCT Number: 2014-000993-20 Sponsor Protocol Number: TW77 Start Date*: 2014-12-04
    Sponsor Name:Center for Research and Development Uppsala University/County Council of Gävleborg
    Full Title: Dosing of intraarticular triamcinolone hexacetonid for knee synovitis in chronic polyarthritis
    Medical condition: Psoriatic arthritis and rheumatoid arthritis with synovitis of the knee
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2013-004512-22 Sponsor Protocol Number: TKSW Start Date*: 2014-03-25
    Sponsor Name:Tays
    Full Title: Treatment of keloidscars with intralesional triamcinolone and 5-fluorouracil injections - prospective, randomized, controlled trial- pilot stydy
    Medical condition: Keloidscars
    Disease: Version SOC Term Classification Code Term Level
    16.1 100000004858 10023329 Keloid LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2017-003205-18 Sponsor Protocol Number: Cingal17-02 Start Date*: 2018-01-26
    Sponsor Name:Anika Therapeutics, Inc.
    Full Title: Extension Study to Cingal 16-02: Trial Extension to 39 Week Follow Up in the Randomized, Double-Blind, Active Comparator Controlled, Multi-Center Study of a Single Injection Cross-Linked Sodium Hya...
    Medical condition: Osteoarthritis of the Knee
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004859 10031165 Osteoarthritis knee LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: PL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2017-000355-46 Sponsor Protocol Number: Cingal16-02 Start Date*: 2017-07-12
    Sponsor Name:Anika Therapeutics, Inc.
    Full Title: A Randomized, Double-Blind, Active Comparator Controlled, Multi-Center Study of a Single Injection Cross-Linked Sodium Hyaluronate Combined with Triamcinolone Hexacetonide (Cingal®) to Provide Symp...
    Medical condition: Osteoarthritis of the Knee
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004859 10031165 Osteoarthritis knee LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: PL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2019-000889-38 Sponsor Protocol Number: 2019/MyJIA Start Date*: 2020-09-16
    Sponsor Name:Oslo University Hospital
    Full Title: Strategies towards personalised treatment in Juvenile Idiopathic Arthritis (JIA): An open randomised multicentre blinded-assessor trial assessing the effectiveness of intra-articular glucocortico...
    Medical condition: Juvenile idiopathic arthritis is characterised by inflamed joints and is the most common chronic rheumatic disease in childhood and adolescence that potentially lead to disability due to joint dama...
    Disease:
    Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: NO (Trial now transitioned)
    Trial results: (No results available)
    EudraCT Number: 2021-004756-42 Sponsor Protocol Number: DIA2021-08 Start Date*: 2022-01-25
    Sponsor Name:Diakonhjemmet sykehus
    Full Title: The NOR-CACTUS Trial: A NORwegian trial CompAring treatment strategies for Carpal TUnnel Syndrome
    Medical condition: Carpal tunnel syndrome - median neuropathy caused by nerve entrapment at the site of the carpal tunnel in the wrist
    Disease: Version SOC Term Classification Code Term Level
    20.0 10029205 - Nervous system disorders 10007697 Carpal tunnel syndrome PT
    21.1 10042613 - Surgical and medical procedures 10007696 Carpal tunnel release LLT
    20.0 10042613 - Surgical and medical procedures 10007695 Carpal tunnel decompression PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NO (Trial now transitioned)
    Trial results: (No results available)
    EudraCT Number: 2015-002343-34 Sponsor Protocol Number: KALK1183 Start Date*: 2015-10-15
    Sponsor Name:Martina Hansens Hospital
    Full Title: Treatment of calcific tendinitis of the Rotator Cuff A randomized, double blinded, sham controlled, international, multicenter study
    Medical condition: Calcific tendinitis of the shoulder
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NO (Completed)
    Trial results: (No results available)
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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