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Phase 2 Completed N=40 Randomized Triple-blind Treatment

Research Investigation of Soy and Estrogen

Menopause · Hot Flashes
Source: ClinicalTrials.gov NCT00997893 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcomePrimary: Change in STAI-6 Score — 12.31; 11.85; 10.76; 11.69 score on STAI scale — p=.004

Summary

The purpose of this study is to determine the effects of oral estradiol and soy phytoestrogens on anxiety, stress responsivity and cognition in perimenopausal women.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in STAI-6 Score
12.31; 11.85; 10.76; 11.69; 11.38; 11.24 .004 sig
PRIMARY
Changes in STAI-6 Scores Before and After Psychosocial Stressor Over Time
8.73; 8.69; 9.77; 12.61; 12.92; 12.23 .98
PRIMARY
Memory for Emotionally Valent Words and Neutral Words
0.45; 0.45; 0.38; 0.48; 0.40; 0.47 .68
PRIMARY
Change in Verbal Memory, Immediate Recall
-.02; 2.31; 2.08 .11
PRIMARY
Change in Verbal Memory, Delayed Recall
.87; 1.61; 1.08 .86

Eligibility Criteria

Inclusion Criteria

  • Female
  • Perimenopausal as defined by the Stages of Reproductive Aging Workshop (STRAW) criteria, specifically in either of the two following stages: a) early transition defined as changes in cycle length of seven days or more in either direction in consecutive cycles or b) late transition defined as > 60 days amenorrhea and FSH > 40 IU/mL
  • Intact uterus/ovaries (i.e. no surgical menopause)
  • at least 1 self-reported hot flash per week
  • Estrogen therapy not contraindicated
  • Able to give informed consent
  • Age between 40 and 65 years
  • English as first and primary language

Exclusion Criteria

  • Positive pregnancy test or breastfeeding (pregnancy tests will be given to all women)
  • Obesity > 35 BMI
  • Previous history of endometrial hyperplasia/neoplasia
  • Previous history of cancers of the breast or reproductive tract
  • History of presence of myocardial infarction (MI) or stroke
  • Current clinical diagnosis or a diagnosis within the past year of an anxiety disorder, severe recurrent depression, or severe psychiatric disturbance
  • History of head injury with more than 60 minutes loss of consciousness
  • History of neurological condition affecting cognitive function (e.g., brain tumor, multiple sclerosis)
  • History of developmental disability affecting cognitive function (e.g., mental retardation, attention deficit)
  • Current use of CNS-acting medication (e.g., antidepressants, anxiolytics, diphenhydramine)
  • History or presence of cerebrovascular accident, sickle cell anemia
  • History of alcohol or drug abuse as defined by DSM criteria
  • Abnormal vaginal bleeding of undetermined cause
  • Untreated or uncontrolled hypertension defined as systolic blood pressure greater than 165 mm hg or diastolic blood pressure greater than 95 mm hg
  • Concurrent administration of medication containing estrogen, progestin, SERM within four months of enrollment
  • Concurrent administration of medication containing St. John's wort, bisphosphonates, or dietary phytoestrogens within one month of enrollment
  • History of migraine associated with hormone use
  • History or presence of deep vein thrombosis, thrombophlebitis or thromboembolic disorder
  • Current participation in any other clinical trial within 30 days of enrollment
  • Smoker
  • Diabetes
  • Premature ovarian failure (defined as having last menstrual period before age 40)
  • Abnormal PAP smear in previous year
  • Abnormal mammogram in previous year
  • Vegans (vegetarians who tend to consume greater than average doses of phytoestrogens)
  • Allergy to soy (affects ~1% of people in the United States; reactions are typically mild)
  • Symptomatic fibroids (significant size or significant menstrual changes)
  • Menorrhagia
  • Lactose intolerant
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00997893). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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