Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-08T08:38:57.909Z Has data issue: false hasContentIssue false

Effectiveness of Harpagophytum extract WS 1531 in the treatment of exacerbation of low back pain: a randomized, placebo-controlled, double-blind study

Published online by Cambridge University Press:  16 August 2006

S. Chrubasik
Affiliation:
Sektion Allgemeinmedizin, Department of Internal Medicine I, Bergheimerstr. 147, 69117 Heidelberg Germany
H. Junck
Affiliation:
Sektion Allgemeinmedizin, Department of Internal Medicine I, Bergheimerstr. 147, 69117 Heidelberg Germany
H. Breitschwerdt
Affiliation:
Department of Medical Biometry, Im Neuenheimer Feld 305, University of Heidelberg, 69120 Heidelberg, Germany
Ch. Conradt
Affiliation:
Department of Medical Biometry, Im Neuenheimer Feld 305, University of Heidelberg, 69120 Heidelberg, Germany
H. Zappe
Affiliation:
Sektion Allgemeinmedizin, Department of Internal Medicine I, Bergheimerstr. 147, 69117 Heidelberg Germany
Get access

Abstract

Two daily doses of oral Harpagophytum extract WS 1531 (600 and 1200, respectively, containing 50 and 100 mg of the marker harpagoside) were compared with placebo over 4 weeks in a randomized, double-blind study in 197 patients with chronic susceptibility to back pain and current exacerbations that were producing pain worse than 5 on a 0–10 visual analogue scale. The principal outcome measure, based on pilot studies, was the number of patients who were pain free without the permitted rescue medication (tramadol) for 5 days out of the last week. The treatment and placebo groups were well matched in physical characteristics, in the severity of pain, duration, nature and accompaniments of their pain, the Arhus low backpain index and in laboratory indices of organ system function. A total of 183 patients completed the study. The numbers of pain-free patients were three, six and 10 in the placebo group (P), the Harpagophytum 600 group (H600) and the Harpagophytum 1200 group (H1200)respectively (P=0.027, one-tailed Cochrane–Armitage test). The majority of responders’ were patients who had suffered less than 42 days of pain, and subgroup analyses suggested that the effect was confined to patients with more severe and radiating pain accompanied by neurological deficit. However, subsidiary analyses, concentrating on the current pain component of the Arhus index, painted a slightly different picture, with the benefits seeming, if anything,to be greatest in the H600 group and in patients without more severe pain, radiation or neurological deficit. Patients with more pain tended to use more tramadol, but even severe and unbearable pain would not guarantee that tramadol would be used at all, and certainly not to the maximum permitted dose. There was no evidence for Harpagophytum-related side-effects, except possibly for mild and infrequent gastrointestinal symptoms.

Type
Original Article
Copyright
1999 European Society of Anaesthesiology

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)