Skip to main content
Log in

Comparison of the Analgesic Effects of a Fixed-Dose Combination of Orphenadrine and Diclofenac (Neodolpasse®) with its Single Active Ingredients Diclofenac and Orphenadrine

A Placebo-Controlled Study Using Laser-Induced Somatosensory-Evoked Potentials from Capsaicin-Induced Hyperalgesic Human Skin

  • Original Research Article
  • Published:
Drugs in R & D Aims and scope Submit manuscript

Abstract

Objective: The aim of this study was to investigate the analgesic efficacy of Neodolpasse®, a fixed-dose combination of orphenadrine and diclofenac, compared with those of its single active ingredients in a human pain model.

Methods: The study was designed as a randomised, double-blind, placebo-controlled, four-period crossover study. Twenty-four healthy female and male subjects received single infusions of Neodolpasse®, orphenadrine, diclofenac or saline solution over 60 minutes. Infusions were separated by a 1-week washout period. Neurogenic inflammation and hyperalgesia were induced by topical occlusive application of a 1% capsaicin solution for 30 minutes on defined skin areas on the back. The pain response to CO2 laser pulses applied to the capsaicin- pretreated skin was measured by event-related vertex EEG recordings. This allowed us to study the influence of a single infusion on the central P2- and peripheral N1-components of laser-induced somatosensory-evoked potentials (LSEP) as a measure of pain response.

Results: Although none of the active treatments had a significant effect on the peripheral N1-component, all active treatments reduced the P2-component of the LSEP, reflecting central/spinal analgesic (anti-hyperalgesic) effects. These effects were statistically significant for orphenadrine (p < 0.0001) and for the combination of orphenadrine and diclofenac (p < 0.0013). The single ingredient diclofenac reduced the P2-component by a value just below clinical relevance (p < 0.0848).

Conclusion: This study demonstrated the efficacy of Neodolpasse® in a human pain model. The observed effect was mainly caused by central mechanisms and was found to be superior for the fixed-dose combination of orphenadrine and diclofenac compared with the individual ingredients. Both components contributed to the effect of the combination in an additive fashion, which can be explained by the different molecular mechanisms of action of each drug.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Table I
Table II
Table III
Fig. 3
Table IV
Table V

Similar content being viewed by others

Notes

  1. The use of trade names is for product identification purposes only and does not imply endorsement.

References

  1. Menasse R, Hedwall PR, Kraetz J, et al. Pharmacological properties of diclofenac sodium and its metabolites. Scand J Rheumatol Suppl 1978; 22: 5–16

    Article  PubMed  CAS  Google Scholar 

  2. Ku EC, Lee W, Kothari HV, et al. Effect of diclofenac sodium on the arachidonic acid cascade. Am J Med 1986; 80: 18–23

    Article  PubMed  CAS  Google Scholar 

  3. Todd PA, Sorkin EM. Diclofenac sodium: a reappraisal of its pharmacodynamic and pharmacokinetic properties, and theraperpeutic cacy. Drugs 1988; 35: 244–85

    Article  PubMed  CAS  Google Scholar 

  4. Jurna I, Brune K. Central effect of the non-steroid anti-inflammatory agents, indomethacin, ibuprofen, and diclofenac, determined in C fibre-evoked activity in single neurones of the rat thalamus. Pain 1990; 41: 71–80

    Article  PubMed  CAS  Google Scholar 

  5. Bijlsma UG, Harms AF, Funcke ABH, et al. The pharmacology of gB-dimethylaminoethyl-2-methylbenzhydrylether hydrochloride. Arch Int Pharmacodyn Ther 1956; 1: 332–68

    Google Scholar 

  6. Ginzel KH. The blockade of reticular and spinal facilitation of motor function by orphenadrine. J Pharmacol Exp Ther 1966; 154: 128–41

    PubMed  CAS  Google Scholar 

  7. Onuaguluchi G, Lewis JJ. Some aspects of the pharmacology of orphenadrine. J Pharm Pharmacol 1963; 15: 329–36

    Article  PubMed  CAS  Google Scholar 

  8. Smith CM. Relaxation of decerebrate rigidity by orphenadrine. Proc Soc Exp Biol Med 1964; 116: 75–6

    PubMed  CAS  Google Scholar 

  9. Steinbrecher W. Myotonolyse durch Orphenadrincitrat. Arzneimittel Forschung 1966; 16: 147–53

    PubMed  CAS  Google Scholar 

  10. Hunskaar S, Donell D. Clinical and pharmacological review of the efficacy of orphenadrine and its combination with paracetamol in painful conditions. J Int Med Res 1991; 19: 71–87

    PubMed  CAS  Google Scholar 

  11. Schaffler K, Reitmeir P. Analgesic effects of low-dose intravenous orphenadrine in the state of capsaicin hyperalgesia: a randomized, placebo-controlled, double-blind cross-over study: using laser somatosensory evoked potentials obtained from capsaicin-irritated skin in healthy volunteer. Arzneimittel Forschung 2004; 54: 673–9

    PubMed  CAS  Google Scholar 

  12. Winter L, Post A. Analgesic combinations with orphenadrine in oral post surgical pain. J Int Med Res 1979; 7: 240–6

    PubMed  Google Scholar 

  13. Raffa RB. Antihistamines as analgesics. J Clin Pharm Ther 2001; 26: 81–5

    Article  PubMed  CAS  Google Scholar 

  14. Olsen UB, Eltorp CT, Ingvardsen BK, et al. ReN 1869, a novel tricyclic antihistamine, is active against neurogenic pain and inflammation. Eur J Pharmacol 2002; 435: 43–57

    Article  PubMed  CAS  Google Scholar 

  15. Jones B, Kenward MG. Design and analysis of cross-over trials. London: Chapman and Hall, 1989

    Google Scholar 

  16. Schaffler K, Wauschkuhn CH, Gierend M. Analgesic potency of a new anticonvulsant drug versus acetylsalicylic acid via laser somatosensory evoked potentials: randomised placebo-controlled double blind (5-way) crossover study. Arzneimittel Forschung 1991; 41: 427–35

    PubMed  CAS  Google Scholar 

  17. Schaffler K, Seibel K, Thomsen M, et al. Effect of the new H1-antagonist ReN1869 on capsaicin-induced hyperalgesia in human skin/Human phase-I trial using somatosensory evoked potentials induced by a CO2 laser. Arzneimittel Forschung 2004; 54: 187–91

    PubMed  CAS  Google Scholar 

  18. Schaffler K, Wauschkuhn CH, Brunnauer H, et al. Evaluation of the local anaesthetic activity of dimethindene maleate by means of laser algesimetry in healthy volunteers. Arzneimittel Forschung 1992; 42: 1332–5

    PubMed  CAS  Google Scholar 

  19. Schaffler K, Medert G. The analgesic, anti-inflammatory profile of dexketoprofen trometamol (vs tramadol). Schmerz 1998; 12 (S1): 69–70

    Google Scholar 

  20. Bromm B, Jahnke MT, Treede RD. Responses of human cutaneous afferents to CO2 laser stimuli causing pain. Exp Brain Res 1984; 55: 158–66

    Article  PubMed  CAS  Google Scholar 

  21. Putt M, Chinchilli VM. A mixed effects model for the analysis of repeated measures cross-over studies. Stat Med 1999; 18: 3037–58

    Article  PubMed  CAS  Google Scholar 

  22. Zecca L, Ferrario P, Costi P. Determination of diclofenac and its metabolites in plasma and cerebrospinal fluid by high-performance liquid chromatography with electrochemical detection. J Chromatogr 1991; 567: 425–32

    Article  PubMed  CAS  Google Scholar 

  23. Valtonen EJ. A controlled clinical trial of chlormezanone, orphenadrine, orphenadrine/paracetamol and placebo in the treatment of painful skeletal muscle spasms. Ann Clin Res 1975; 7: 85–8

    PubMed  CAS  Google Scholar 

  24. Hough LB, Nalwalk JW, Svokos K, et al. Pain-relieving drugs and the brain histaminergic system: multiple analgesic mechanisms from histamine, improgan and cimetidine. Inflamm Res 2004; 53 Suppl. 1: S43–4

    Article  Google Scholar 

  25. Kashiba H, Fukui H, Senba E. Histamine H1 receptor mRNA is expressed in capsaicin-insensitive sensory neurons with neuropeptide Y-immunoreactivity in guinea pigs. Brain Res 2001; 901: 85–93

    Article  PubMed  CAS  Google Scholar 

  26. Diamond BI, Bluhm RE, Borison RL, et al. Brain histamine: an endogenous system for mediating pain [abstract]? Anaesthesiology 1981; 55: A286

    Article  Google Scholar 

  27. Eguiagaray JG, Egea J, Bravo-Cordero JJ, et al. Neurotransmisores, senales de calcio y comunication neuronal [Neurotransmitters, calcium signalling and neuronal communication]. Neurocirugia 2004; 15: 109–18

    PubMed  CAS  Google Scholar 

  28. Vane JR, Bahlke YS, Botting RM. Cyclooxygenases 1 and 2. Annu Rev Pharmacol Toxicol 1998; 38: 97–120

    Article  PubMed  CAS  Google Scholar 

  29. Pinardi G, Sierralta F, Miranda HF. Adrenergic mechanisms in antinociceptive effects of non steroidal anti-inflammatory drugs in acute thermal nociception in mice. Inflamm Res 2002; 51: 219–22

    Article  PubMed  CAS  Google Scholar 

  30. Pinardi G, Sierralta F, Miranda HF. Atropine reverses the antinociception of nonsteroidal anti-inflammatory drugs in the tail-flick test of mice. Pharmacol Biochem Behav 2003; 74: 603–8

    Article  PubMed  CAS  Google Scholar 

  31. Kornhuber J, Parsons CG, Hartmann S, et al. Orphenadrine is an uncompetitive n-methyl-d-aspartate (NMDA) receptor antagonist: binding and patch clamp studies. J Neural Transm Gen Sect 1995; 102: 237–42

    Article  PubMed  CAS  Google Scholar 

  32. Rumore MM, Schlichting DA. Analgesic effects of antihistamines. Life Sci 1985; 36: 403–16

    Article  PubMed  CAS  Google Scholar 

  33. Pubill D, Canudas AM, Pallas M, et al. Assessment of the adrenergic effects of orphenadrine in rat vas deferens. J Pharm Pharmacol 1999; 51: 307–12

    Article  PubMed  CAS  Google Scholar 

  34. Seibel K, Schaffler K, Reeh P, et al. Comparison of two different preparations of ibuprofen with regard to the time course of their analgesic effect: using laser somatosensory evoked potentials from UV-irritated skin in healthy volunteers. Drug Res 2004; 54: 444–51

    CAS  Google Scholar 

Download references

Acknowledgements

The authors wish to thank Gerd Hoerl, PhD and Peter Schaffer, PhD for their valuable contributions in planning this clinical study, and Fresenius Kabi Austria GmbH for financial support for the study. The authors had no other financial support other than that provided by the study sponsor. They have no potential conflicts of interest that are relevant to the contents of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Klaus Schaffler.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schaffler, K., Reitmeir, P., Gschanes, A. et al. Comparison of the Analgesic Effects of a Fixed-Dose Combination of Orphenadrine and Diclofenac (Neodolpasse®) with its Single Active Ingredients Diclofenac and Orphenadrine. Drugs R D 6, 189–199 (2005). https://doi.org/10.2165/00126839-200506040-00001

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2165/00126839-200506040-00001

Keywords

Navigation