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Equine veterinary journal2003; 35(4); 407-413; doi: 10.2746/042516403776014226

Tiludronate as a new therapeutic agent in the treatment of navicular disease: a double-blind placebo-controlled clinical trial.

Abstract: Bisphosphonates, such as tiludronate, are used to normalise bone metabolism via inhibition of bone resorption. Areas of increased bone resorption and formation are typical lesions in a diseased navicular bone. Objective: To determine if bone remodelling changes occurring in navicular disease may be corrected with therapies regulating bone metabolism. Methods: We designed a double-blind, placebo-controlled clinical trial to compare 2 doses of tiludronate, 0.5 mg/kg and 1 mg/kg bwt administered via daily i.v. injections over 10 days for the treatment of navicular disease. Seventy-three horses, split into 2 subpopulations of recent and chronic cases, were enrolled to be followed-up over 6 months. Of these, 33 recent and 17 chronic cases meeting the selection criteria were maintained in the final efficacy analyses. Clinical examinations were videorecorded and reviewed blindly by an independent expert. Results: Horses treated with the higher dose showed optimal improvement of lameness and return to normal level of activity 2-6 months post treatment. The more recent the onset of clinical signs at the time of treatment, the greater the efficacy. The treatment did not modify the response to extension and flexion tests. The lower dose failed to significantly improve the condition. Conclusions: Tiludronate efficacy is demonstrated in the treatment of navicular disease at the dose of 1 mg/kg bwt. Conclusions: Our results support the clinical relevance of bone remodelling changes in the outcome of navicular disease.
Publication Date: 2003-07-26 PubMed ID: 12880010DOI: 10.2746/042516403776014226Google Scholar: Lookup
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  • Clinical Trial
  • Journal Article
  • Randomized Controlled Trial

Summary

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This study evaluates the effectiveness of Tiludronate, a bisphosphonate medication used to regulate bone metabolism, in treating navicular disease in horses. The research indicates that higher doses of Tiludronate lead to significant improvement in lameness symptoms and restore normal activity levels within 2-6 months.

Study Subjects and Methodology

  • The researchers conducted a double-blind, placebo-controlled clinical trial to compare the effects of 0.5 mg/kg and 1 mg/kg doses of Tiludronate administered via daily intravenous injections over a 10-day period.
  • 73 horses, categorised into two groups based on the duration of their illness (recent or chronic), were initially selected to participate.
  • However, only 33 recent and 17 chronic cases that met the selection criteria were included in the final analysis.
  • The horses’ condition was assessed over a 6-month follow-up period. Their clinical examinations were video-recorded and reviewed by an independent expert who was not privy to the treatment details (double-blind).

Key Findings

  • The research found that horses treated with the higher dose (1 mg/kg) showed substantial improvement in their lameness conditions and returned to their previous activity levels between 2-6 months after treatment.
  • The study also found out that the quicker the treatment was started after the initial onset of symptoms, the greater the efficacy of the treatment.
  • This treatment, however, did not alter the horses’ responses to extension and flexion tests.
  • The lesser dose of 0.5 mg/kg was not found to significantly improve the condition of the horses.

Conclusions

  • Implications of the study show that Tiludronate effectively treats navicular disease at a dosage level of 1 mg/kg body weight.
  • The researchers also observe that the changes in bone remodelling have a significant clinical impact on the outcome of navicular disease.

Cite This Article

APA
Denoix JM, Thibaud D, Riccio B. (2003). Tiludronate as a new therapeutic agent in the treatment of navicular disease: a double-blind placebo-controlled clinical trial. Equine Vet J, 35(4), 407-413. https://doi.org/10.2746/042516403776014226

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 35
Issue: 4
Pages: 407-413

Researcher Affiliations

Denoix, J M
  • CIRALE/ENVA IPC, Goustranville, 14430 Dozulé, France.
Thibaud, D
    Riccio, B

      MeSH Terms

      • Animals
      • Bone Resorption / drug therapy
      • Bone Resorption / veterinary
      • Diphosphonates / therapeutic use
      • Dose-Response Relationship, Drug
      • Double-Blind Method
      • Female
      • Foot Diseases / drug therapy
      • Foot Diseases / veterinary
      • Hoof and Claw
      • Horse Diseases / drug therapy
      • Horses
      • Injections, Intravenous / veterinary
      • Lameness, Animal / drug therapy
      • Male
      • Osteitis / drug therapy
      • Osteitis / veterinary
      • Treatment Outcome
      • Video Recording

      Citations

      This article has been cited 15 times.
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