2001
DOI: 10.1002/ptr.898
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Efficacy and tolerance of Harpagophytum extract LI 174 in patients with chronic non‐radicular back pain

Abstract: The aim of this open, multicentre study was to evaluate the clinical effectiveness and tolerance of the Devil's Claw extract LI 174 in patients suffering from non-radicular back pain over a period of at least 6 months. A total of 130 patients were treated twice a day with tablets containing 480 mg LI 174. The treatment lasted for 8 weeks. The effectiveness was judged according to the Multidimensional Pain Scale (MPS), Arhus back pain index and to parameters evaluating the mobility of the lumbar spine (finger-f… Show more

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Cited by 25 publications
(7 citation statements)
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“…Data on Harpagophytum efficacy from other studies can therefore not be transferred to extract LI 174 unless its bioequivalence (through bioavailability) to the extracts used in those studies has been demonstrated (Chrubasik and Roufogalis, 2001). Although presented as a high-dose Harpagophytum extract (Laudahn and Walper, 2001), extract LI 174 conforms only to the German Commission E Monograph (Blumenthal, 1998), with the daily dose being equivalent to 4.5 g crude plant material, rather than the ESCOP monograph, which recommends a higher dose -up to 9 g per day (Anon., 1996). The drug -LI 174 extract ratio does not reflect the final content of the coactive compound harpagoside (Sporer and Chrubasik, 1999).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Data on Harpagophytum efficacy from other studies can therefore not be transferred to extract LI 174 unless its bioequivalence (through bioavailability) to the extracts used in those studies has been demonstrated (Chrubasik and Roufogalis, 2001). Although presented as a high-dose Harpagophytum extract (Laudahn and Walper, 2001), extract LI 174 conforms only to the German Commission E Monograph (Blumenthal, 1998), with the daily dose being equivalent to 4.5 g crude plant material, rather than the ESCOP monograph, which recommends a higher dose -up to 9 g per day (Anon., 1996). The drug -LI 174 extract ratio does not reflect the final content of the coactive compound harpagoside (Sporer and Chrubasik, 1999).…”
Section: Resultsmentioning
confidence: 99%
“…The open uncontrolled study by Laudahn and Walper (2001) does at most indicate a trend of efficacy, potential confounders were not considered. Clinical efficacy can only be proven in a confirmatory study.…”
Section: Resultsmentioning
confidence: 99%
“…Laudahn and Walper (2001) carried out an uncontrolled trial with 130 patients suffering from chronic non-radicular back pain that had lasted for at least 6 months prior to recruitment. The study lasted for 8 weeks with the administration of a daily dose of 960 mg Hp preparation.…”
Section: Chronic Non-specific Back Painmentioning
confidence: 99%
“…This study was designed specifically to investigate the effectiveness and safety of Hp tablets in the treatment of patients with general rheumatic disorders, monitoring a variety of biochemical and clinical parameters. Although other open studies have been carried out using aqueous Hp (Grahame and Robinson, 1981;Laudahn and Walper, 2001;Wegener and Lupke, 2003) none has looked at the influence of Hp on different joints, measured tolerance and safety parameters and assessed patient satisfaction.…”
Section: Introductionmentioning
confidence: 98%