Triamcinolone hexacetonide 100mg/5ml suspension for injection vials
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1 branded products available
WHO defined daily dose (DDD)
7.5 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
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Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 6 · Randomised trials: 14 · 1972–2026
Showing the 50 most relevant studies, sorted by most relevant.
Mark C. Gillies
Archives of Ophthalmology, 2003
Bensa A, Salerno M, Moraca G, et al.
2024
PurposeThe purpose of this study was to quantify and compare the clinical relevance of the different intra-articular corticosteroids (CS) effects in vivo for osteoarthritis (OA) treatment.MethodsThe search was conducted on PubMed, Cochrane, and Web of Science in October 2023. The PRISMA guidelines were used. Inclusion criteria: animal or human randomized controlled trials (RCTs), English language and no time limitation, on the comparison of different intra-articular CS for OA treatment. The articles' quality was assessed using the Cochrane RoB2 and GRADE guidelines for human RCTs, and SYRCLE's tool for animal RCTs.ResultsEighteen RCTs were selected (16 human and 2 animal studies), including 1577 patients (1837 joints) and 31 animals (51 joints). The CS used were triamcinolone (14 human and 2 animal studies), methylprednisolone (7 human and 1 animal study), betamethasone (3 human studies) and dexamethasone (1 human study). All studies addressed knee OA except for three human and one animal study. A meta-analysis was performed on the comparison of methylprednisolone and triamcinolone in humans with knee OA analysing VAS pain at very short- (≤2 weeks), short- (>2 and ≤4 weeks), mid- (>4 and ≤8 weeks), long- (>8 and ≤ 12 weeks), and very long-term (>12 and ≤24 weeks). Triamcinolone showed better post-injection values compared to methylprednisolone at very short-term (p = 0.028). No difference in terms of VAS improvement was observed at any follow-up.ConclusionsThe available preclinical and clinical literature provides limited evidence on the comparison of different CS, hindering the possibility of determining the best CS approach in terms of molecule and dose for the intra-articular injection of OA joints.Level of evidenceLevel I.
Abstract licence: CC BY
Gallizzi R, Dipasquale RF, Mendicino A, et al.
2025
- Adrenal Cortex Hormones
- Glucocorticoids
- Arthritis, Juvenile
IntroductionJuvenile idiopathic arthritis (JIA) is the most common rheumatic disease of childhood, and steroid intra-articular injections are a fundamental treatment modality among local therapeutic interventions. The aim of this systemic review was to assess the scientific evidence on the effectiveness and safety of intra-articular corticosteroids (IACS) injections, focusing on a comparative examination of the different therapeutic options.Material and methodsPubMed, Scopus, and Web of Science were systematically searched from the inception until February 25, 2025, to identify observational studies presenting participants with a diagnosis of JIA, IACS injections for joints affected by arthritis as interventions, and clinical or radiological assessment of arthritis as outcomes.ConclusionsFindings from this systematic review suggested that IACS injections might be effective in improving arthritis in patients affected by JIA, with good evidence of safety. Moreover, the review underlines a higher efficacy of triamcinolone hexacetonide among corticosteroids used for injections. Further studies with a higher level of evidence and more representative samples should be conducted. What is Known: • Juvenile idiopathic arthritis is the most prevalent chronic rheumatic condition in childhood and represents a major cause of disability. • The management of juvenile idiopathic arthritis involves a variety of therapeutic modalities, among which intra-articular corticosteroid injections.What is new• Intra-articular corticosteroid injections induce rapid symptom control and prolonged remission in a substantial proportion of patients. • Among different types of corticosteroids, triamcinolone hexacetonide is more effective in prolonging remission duration in JIA.
Abstract licence: CC BY
L. Hangody, Róbert Sződy, P. Łukasik, et al.
Cartilage, 2017
- Anti-Inflammatory Agents
- Combined Modality Therapy
- Hyaluronic Acid
José Carlos Nunes-Tamashiro, Jamil Natour, Fernando Maier Ramuth, et al.
Clinical Rehabilitation, 2022
- Osteoarthritis, Knee
- Platelet-Rich Plasma
- Saline Solution
Gustavo Constantino de Campos, Márcia Uchôa de Rezende, Alexandre Felício Pailo, et al.
Clinical Orthopaedics and Related Research, 2012
- Glucocorticoids
- Injections, Intra-Articular
- Pain
Yendrembam Anamika Chanu, Naorem Bimol, Shanavas Anoth Meethal, et al.
Journal of Medical Society, 2025
Wuppi Miku, N. Bimol, Yendrembam Anamika Chanu, et al.
International Journal of Science and Research (IJSR), 2026
Mehrzad Hajialilo, Amir Ghorbanihaghjo, Leyla Valaee, et al.
Clinical Rheumatology, 2016
- Arthrocentesis
- Anti-Inflammatory Agents
- Arthritis, Rheumatoid
K. Gaffney, J. Ledingham, J. D. Perry
Annals of the Rheumatic Diseases, 1995
- Knee Joint
- Administration, Topical
- Anti-Inflammatory Agents
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.