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Study to determine the efficacy and onset of Bonipar, a topical analgesic for the management of acute and chronic musculoskeletal pain.
Roy, Lance A; Li, Yi-Ju; Feliu, Miriam H; Bloomfield, Andrew; Parris, Winston C V.
Afiliación
  • Roy LA; Department of Anesthesiology, Duke University School of Medicine, Durham, NC, USA; Anesthesiology Service, Durham VA Medical Center, Durham, NC, USA. Electronic address: lance.roy@duke.edu.
  • Li YJ; Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.
  • Feliu MH; Department of Psychiatry, Duke University School of Medicine, Durham, NC, USA.
  • Bloomfield A; Department of Anesthesiology, Duke University School of Medicine, Durham, NC, USA.
  • Parris WCV; Department of Anesthesiology, Duke University School of Medicine, Durham, NC, USA.
Complement Ther Clin Pract ; 57: 101908, 2024 Sep 15.
Article en En | MEDLINE | ID: mdl-39293126
ABSTRACT

BACKGROUND:

Opioid abuse and mortality are ravaging American society, highlighting the need to find alternative effective analgesics with fewer side effects. FDA-approved topical analgesics, including non-steroidal anti-inflammatory drugs (NSAIDs), are commonly used to treat musculoskeletal pain but can cause adverse effects. Natural compounds, including essential oils, are potential therapeutic alternatives for managing musculoskeletal pain. If these compounds can provide comparable analgesia to FDA-approved products, it will increase the available options for people with pain, improving quality of life with minimal morbidity and mortality.

OBJECTIVE:

This study assesses the effectiveness and onset of action of Bonipar, a topical analgesic formulated with camphor, methyl salicylate, and oils of coconut, eucalyptus, nutmeg, and rosemary, in managing musculoskeletal pain compared to 1.5 % diclofenac solution, an FDA-approved topical non-steroidal anti-inflammatory drug.

METHODS:

One hundred sixty-four adult patients with localized musculoskeletal pain were randomly assigned to twice-daily applications of either Bonipar or Diclofenac for one week. The primary outcome measure was a 50 % reduction in pain after one week. Secondary outcomes included the change in pain from baseline and onset of action, defined as the first reduction in pain by 20 %.

RESULTS:

All patients completed the initial pain assessment to determine the onset of action. One-week data was available for 74 patients treated with diclofenac and 72 patients treated with Bonipar. Data for 18 patients were incomplete. The proportion of patients achieving a 50 % reduction in pain was statistically similar between the two groups. The success rates of achieving a 50 % pain reduction with Bonipar were found to be non-inferior to those treated with diclofenac. All follow-up time points showed roughly similar results between the groups. Regression models adjusted for age and sex revealed no significant effects on pain changes. Secondary analyses demonstrated no significant differences between the groups.

DISCUSSION:

The topical analgesic Bonipar demonstrates a comparable onset of action, with efficacy non-inferior to diclofenac in the management of musculoskeletal pain, while showing fewer adverse effects compared to diclofenac. These findings highlight the potential of Bonipar as a valuable alternative for the treatment of localized pain.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Complement Ther Clin Pract Asunto de la revista: ENFERMAGEM / OBSTETRICIA / PERINATOLOGIA / TERAPIAS COMPLEMENTARES Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Complement Ther Clin Pract Asunto de la revista: ENFERMAGEM / OBSTETRICIA / PERINATOLOGIA / TERAPIAS COMPLEMENTARES Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido