Intramuscular neridronate for the treatment of complex regional pain syndrome type 1: a randomized, double-blind, placebo-controlled study

Author:

Varenna Massimo1ORCID,Braga Vania2,Gatti Davide3,Iolascon Giovanni4,Frediani Bruno5,Zucchi Francesca6,Crotti Chiara6ORCID,Nannipieri Fabrizio7,Rossini Maurizio3ORCID

Affiliation:

1. Bone Diseases Unit, Department of Rheumatology, Gaetano Pini Institute, Via Pini, 9, Milan 20122, Italy

2. ULSS 9, Verona, Italy

3. Rheumatology Unit, Department of Medicine, University of Verona, Verona, Veneto, Italy

4. Department of Medical and Surgical Specialties, University of Campania “Luigi Vanvitelli”, Naples, Italy

5. Unit of Rheumatology, University of Siena, Siena, Toscana, Italy

6. Bone Diseases Unit, Department of Rheumatology, Gaetano Pini Institute, Milan, Italy

7. Clinical Research, Abiogen Pharma, Pisa, Toscana, Italy

Abstract

Background: Complex regional pain syndrome type-1 (CRPS-1) is a severely disabling painful disease challenging to treat. This multicenter, randomized, double-blind placebo-controlled trial examined the efficacy of intramuscular (i.m.) neridronate in CRPS-1 patients. Methods: A total of 78 patients diagnosed with CRPS-1 (aged 59.5 ± 10.3, 66.7% female) were randomly assigned to 25 mg (i.m.) neridronate ( N = 41) given once daily for 16 consecutive days or placebo control ( N = 37). Efficacy was assessed after 30 days using a visual analogue scale (VAS) pain score and the number of patients achieving ⩾50% reduction in VAS score. Change in clinical signs and symptoms, quality of life (QoL) using Short Form Health Survey (SF-36) and the McGill Pain Questionnaire were also assessed. Results: After 30 days, VAS score decreased significantly to a greater extent in neridronate-treated patients versus placebo (31.9 ± 23.3 mm versus 52.3 ± 27.8 mm, p = 0.0003). Furthermore, the proportion of patients achieving a VAS reduction of ⩾50% was greater in the neridronate group (65.9% versus 29.7%, p = 0.0017). Clinical signs and symptoms were improved significantly in the neridronate group versus placebo for edema (72.5% versus 79.9%, p = 0.03), pain during motion (70% versus 83.3%, p = 0.0009), allodynia (20% versus 63.3%, p = 0.0004), and hyperalgesia (20% versus 56.7%, p = 0.0023). Whereas no difference was observed for QoL measures using the SF-36 questionnaire, three of the four pain variables using the McGill Pain Questionnaire improved significantly in the neridronate group. No serious drug-related adverse events were reported during the study. Conclusion: In patients with acute CRPS-1, i.m. injections of 25 mg neridronate were associated with clinically relevant benefit compared with placebo controls. Trial registration: EU Clinical Trials Register: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2014-001156-28

Funder

Abiogen Pharma S.p.A, Pisa, Italy.

Publisher

SAGE Publications

Subject

Orthopedics and Sports Medicine,Rheumatology

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