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. Author manuscript; available in PMC: 2007 Aug 1.
Published in final edited form as: Climacteric. 2006 Aug;9(4):245–263. doi: 10.1080/13697130600736934

Table 4.

Randomized, Controlled Trials of Red Clover for bone in postmenopausal women

Author, year Design Subjects Intervention type and duration Outcome
Clifton-Bligh, 2001 42 RCT with 3 groups. One month of placebo period followed by 6 months of treatment and 1 month of placebo washout. Placebo periods were single blinded.
  • Postmenopausal women

  • Mean age range 55–59

  • n=46

The three doses of Rimostil were: 28 mg/d, 57 mg/d, and 85.5 mg/d of isoflavones.
Duration: 6 months
BMD of radius and ulna increased significantly for women in medium and high treatment groups.
Safety: endometrial thickness did not change significantly during treatment.
Atkinson, 2004 45 RCT with 2 groups: Placebo or isoflavone tablet
  • Pre, peri, and postmenopausal women

  • Ages 49–65

  • N=205

Promensil tablet was uses as treatment. One tablet per day in intervention group.
Duration: 12 months
Loss of lumbar spine BMC and BMD significantly lower in women taking supplement.
Bone formation markers significantly increased in supplement group.
Schult, 2004 43 RCT with 3 groups: Promensil®, Rimostil®, and placebo
  • Perimenopausal women

  • Ages 45 to 60

  • n=250

Promensil: Red clover extract with 41 mg isoflavones per tablet
Rimostil: Red clover extract with 28.6 mg isoflavones per tablet.
Two tablets per day of each treatment.
Duration: 12 weeks
No significant differences between groups in bone turnover markers
*

Abbreviations: RCT=Randomized Controlled Trial, BMD=bone mineral density, BMC=bone mineral content