Guest guest Posted October 26, 2005 Report Share Posted October 26, 2005 Hi All, See the below suggesting that ginseng extract reduces cold in symptoms and number. http://www.cbc.ca/story/science/national/2005/10/24/cold051024.html Efficacy of an extract of North American ginseng containing poly-furanosyl-pyranosyl-saccharides for preventing upper respiratory tract infections: a randomized controlled trial Gerald N. Predy, Vinti Goel, Ray Lovlin, Allan Donner, Larry Stitt, and Tapan K. Basu CMAJ 2005 173: 1043-1048. Methods: We conducted a randomized, double-blind, placebo-controlled study at the onset of the influenza season. A total of 323 subjects 18–65 years of age with a history of at least 2 colds in the previous year were recruited from the general population in Edmonton, Alberta. The participants were instructed to take 2 capsules per day of either the North American ginseng extract or a placebo for a period of 4 months. The primary outcome measure was the number of -verified colds. Secondary variables measured included symptom severity, total number of days of symptoms and duration of all colds. Cold symptoms were scored by subjects using a 4-point scale. Results: Subjects who did not start treatment were excluded from the analysis (23 in the ginseng group and 21 in the placebo group), leaving 130 in the ginseng group and 149 in the placebo group. The mean number of colds per person was lower in the ginseng group than in the placebo group (0.68 [standard deviation (SD) 0.82] v. 0.93 [sD 0.91], difference 0.25%, 95% confidence interval [CI] 0.04–0.45). The proportion of subjects with 2 or more -verified colds during the 4-month period (10.0% v. 22.8%, 12.8% difference, 95% CI 4.3–21.3) was significantly lower in the ginseng group than in the placebo group, as were the total symptom score (77.5 [sD 84.6] v. 112.3 [sD 102.5], difference 1.5%, 95% CI 1.2–2.0) and the total number of days cold symptoms were reported (10.8 [sD 9.7] v. 16.5 [sD 13.8] days, difference 1.6%, 95% CI 1.3–2.0) for all colds. .... Results After the screening process, a total of 323 volunteers were enrolled and randomly assigned to the placebo or ginseng group (Fig. 1). Of these, 153 were assigned to receive the ginseng extract and 170 to receive placebo. The treatment assignment imbalance was due to the lack of a blocking factor in the randomization process. Of subjects in the ginseng group, 23 (15.0%) did not start their treatment, and in the placebo group, 21 (12.4%) failed to start. A number of reasons for withdrawal were given, including changing employment, compulsory immunization and holiday commitments. Some withdrew without giving a reason. A total of 130 in the ginseng group and 149 in the placebo group began the treatments and were included in data analysis. Twelve (9.2%) in the ginseng group and 11 (7.4%) in the placebo group discontinued for various reasons (Fig. 1). There were no significant differences in baseline characteristics between the subjects included and those excluded from data analysis (Table 1). The 2 study groups were similar with respect to age, sex and history of colds. Compliance was high in both groups: 90% in the ginseng group and 92% in the placebo group reported taking more than 75% of the medication. Blinding was also maintained adequately during the treatment period. On completion of the study, 69.8% of those taking ginseng and 77.3% of those taking placebo thought they had been given the ginseng extract. The mean number of -verified colds per person was less in the ginseng group than in the placebo group (0.68 v. 0.93, difference 0.25%, 95% confidence interval [CI] 0.04 to 0.45, p = 0.017) (Table 2). Fewer subjects in the ginseng group reported contracting at least 1 cold during the 4-month intervention period than in the placebo group (54.6% [71/130] v. 63.8% [95/149], difference 9.1%, 95% CI –2.4 to 20.7), but the difference was nonsignificant. However, the difference in recurrent colds was significant: 10.0% in the ginseng group reported having more than one cold compared with 22.8% in the placebo group (difference 12.8%, 95% CI 4.3 to 21.3, p = 0.004). Similar results were observed for all colds reported. The total symptom score of all colds during the 4-month intervention period in the ginseng and placebo groups was 77.5 and 112.3 respectively (difference 1.5%, 95% CI 1.2–2.0, p = 0.002) (Table 3). A similar result was obtained when the total symptom scores per cold were compared. The total number of days that cold symptoms were experienced was significantly fewer in the ginseng group (10.8 v. 16.5 days, difference 1.6%, 95% CI 1.3–2.0, p < 0.001). The interventions were generally well tolerated by the subjects (Table 4). The frequency of adverse events was similar in the 2 groups. Type 2 diabetes mellitus was diagnosed in 2 subjects in the ginseng group, and they were subsequently withdrawn from the study. Supplementary medications, particularly NSAIDs, were used by 26.2% (34/130) and 29.5% (44/149) of the subjects in the ginseng and placebo groups respectively. Four (3.1%) in the ginseng group and 5 (3.4%) in placebo reported taking antibiotics for their colds and flu. The differences in the incidence of NSAIDs and antibiotic use between the 2 groups were not found to be statistically significant. ... Al Pater, PhD; email: old542000@... __________________________________ - PC Magazine Editors' Choice 2005 http://mail. Quote Link to comment Share on other sites More sharing options...
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