Safety and efficacy of black cohosh and red clover for the management of vasomotor symptoms: a randomized controlled trial.
- 2009-11
- Menopause (New York, N.Y.) 16(6)
- Stacie E Geller
- Lee P Shulman
- Richard B van Breemen
- Suzanne Banuvar
- Ying Zhou
- Geena Epstein
- Samad Hedayat
- Dejan Nikolic
- Elizabeth C Krause
- Colleen E Piersen
- Judy L Bolton
- Guido F Pauli
- Norman R Farnsworth
- PubMed: 19609225
- DOI: 10.1097/gme.0b013e3181ace49b
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Sample size
- n = 89
- Population
- 89 participants (women with menopausal vasomotor symptoms)
- Methods
- randomized, four-arm, double-blind clinical trial of standardized black cohosh, red clover, placebo, and 0.625 mg conjugated equine estrogens plus 2.5 mg medroxyprogesterone acetate (CEE/MPA)
- Blinding
- Double-blind
- Duration
- 12 months
- Funding
- Unclear
- Highly Cited
Objective
The aim of this study was to evaluate the safety and efficacy of black cohosh and red clover compared with placebo for the relief of menopausal vasomotor symptoms.Methods
This study was a randomized, four-arm, double-blind clinical trial of standardized black cohosh, red clover, placebo, and 0.625 mg conjugated equine estrogens plus 2.5 mg medroxyprogesterone acetate (CEE/MPA; n = 89). Primary outcome measures were reduction in vasomotor symptoms (hot flashes and night sweats) by black cohosh and red clover compared with placebo; secondary outcomes included safety evaluation, reduction of somatic symptoms, relief of sexual dysfunction, and overall improvement in quality of life.Results
Reductions in number of vasomotor symptoms after a 12-month intervention were as follows: black cohosh (34%), red clover (57%), placebo (63%), and CEE/MPA (94%), with only CEE/MPA differing significantly from placebo. Black cohosh and red clover did not significantly reduce the frequency of vasomotor symptoms as compared with placebo. Secondary measures indicated that both botanicals were safe as administered. In general, there were no improvements in other menopausal symptoms.Conclusions
Compared with placebo, black cohosh and red clover did not reduce the number of vasomotor symptoms. Safety monitoring indicated that chemically and biologically standardized extracts of black cohosh and red clover were safe during daily administration for 12 months.Research Insights
In general, there were no improvements in other menopausal symptoms.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
In general, there were no improvements in other menopausal symptoms.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
Reductions in number of vasomotor symptoms after a 12-month intervention were as follows: ... red clover (57%), placebo (63%)... with only CEE/MPA differing significantly from placebo. Black cohosh and red clover did not significantly reduce the frequency of vasomotor symptoms as compared with placebo.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
In general, there were no improvements in other menopausal symptoms.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
In general, there were no improvements in other menopausal symptoms.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
In general, there were no improvements in other menopausal symptoms.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
Reductions in number of vasomotor symptoms after a 12-month intervention were as follows: ... red clover (57%), placebo (63%)... with only CEE/MPA differing significantly from placebo. Black cohosh and red clover did not significantly reduce the frequency of vasomotor symptoms as compared with placebo.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
In general, there were no improvements in other menopausal symptoms.
- Effect
- Neutral
- Effect size
- Small
- Dose
- standardized extract, dose not specified
Adverse Events Reported
Secondary measures indicated that both botanicals were safe as administered.
- Finding
- No significant difference
- Significant
- No
Secondary measures indicated that both botanicals were safe as administered.
- Finding
- No significant difference
- Significant
- No
Safety monitoring indicated that chemically and biologically standardized extracts of black cohosh and red clover were safe during daily administration for 12 months.
- Finding
- Reported
Safety monitoring indicated that chemically and biologically standardized extracts of black cohosh and red clover were safe during daily administration for 12 months.
- Finding
- Reported