Assessing the Synergistic Effects of Black Cohosh, Soy Isoflavones, and SDG Lignans (Soloways TM) on Menopausal Symptoms

Not Applicable

Completed

• Conditions: Menopause Symptoms

• Registration Number: NCT06328348
• Lead Sponsor: S.LAB (SOLOWAYS)

Brief Summary

This clinical trial aimed to evaluate the effectiveness of a combination of Black Cohosh, Soy Isoflavones, and SDG Lignans compared to a placebo in reducing menopausal symptoms in postmenopausal women aged 45-60 years. The study was meticulously designed to be a randomized, double-blind, parallel-group trial, ensuring rigorous scientific standards and participant confidentiality. It received ethical approval and adhered to the Declaration of Helsinki guidelines. Participants were carefully selected based on specific inclusion and exclusion criteria to maintain the study's integrity and relevance to the target population.

The trial involved 96 eligible women from the Center for New Medical Technologies registry in Novosibirsk, Russia, divided into two groups through a computer-generated random sequence. One group received the active supplements, while the other received a placebo, with both groups and researchers blinded to the assignments. The supplements and placebos were produced to be indistinguishable in appearance, with dosages designed to maximize absorption and efficacy while minimizing side effects. The primary endpoint was the change in Menopause Rating Scale (MRS) scores, with secondary outcomes focusing on adverse symptoms and key hormonal changes.

The study's design also included measures to ensure adherence and minimize bias, such as drug container returns and daily reminders. The involvement of S.Lab (Soloways) was limited to manufacturing the supplements, with the research conducted independently to avoid commercial influence. The sample size calculation indicated that 48 participants per group would provide adequate power to detect significant differences in menopausal symptom reduction, aiming for a high level of confidence and statistical power.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-07-18
• Primary Completion: 2023-11-30
• Study Completion: 2023-12-30
• Status Verified: 2024-03
• Study First Submitted: 2024-03-18
• Study First Submitted QC: 2024-03-18
• Last Update Submitted: 2024-03-18
• Study First Posted: 2024-03-25
• Last Update Posted: 2024-03-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 96

Inclusion Criteria

• Time since menopause less than 10 years
• Natural menopause confirmed
• Abstainers from smoking and alcohol consumption
• Normal thyroid function tests and lipid profiles
• Body Mass Index (BMI) within the 18.5-30 kg/m2 range, to ensure a representative sample of the population
• Recent mammography and gynecological examination (within the last year) confirming the absence of breast or reproductive system diseases

Exclusion Criteria

• Contraindications to hormone therapy, including a history of suspected or diagnosed malignancy
• Use of hormonal treatments or products derived from soybeans or cod liver oil within the last 12 months
• Allergies to soybeans or cod liver oil
• Engagement in professional athletic activities
• Current use of medications that may interact with study supplements, including but not limited to sulfonamides, methotrexate, triamterene, sulfasalazine, phenytoin, anxiolytics, antidepressants, as well as daily chemicals, multivitamins, aspirin, or painkillers
• Use of alternative herbal remedies for vasomotor symptoms within the past month
• Participation in another investigational program involving interventions outside of routine clinical practice within the last 6 months
• Presence of uncontrolled hypertension or diabetes, or a significant psychiatric condition that could interfere with study participation
• History of serious cardiovascular diseases, including myocardial infarction or stroke

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in the Menopause Rating Scale (MRS) score	90 days	Each symptom is rated on a scale from 0 (no complaints) to 4 (severe symptoms), leading to a total MRS score that ranges from 0 to 44

Secondary Outcome Measures

Name	Time	Method
Follicle-Stimulating Hormone (FSH) change	90 days
Estradiol change	90 days
Number of any adverse events	90 days	any reported adverse events

Trial Locations

Locations (1)

Center of New Medical Technologies; 🇷🇺 Novosibirsk, Novosibisk Region, Russian Federation