Herbal Dietary Supplementation on Vasomotor Symptoms in Menopausal Women

Part of paid clinical trials in Harrison, New York.

Sponsor
Bonafide Health
Study ID
NCT07408115
Status
Completed

Conditions

  • Hot Flash
  • Hot Flashes
  • Hot Flushes
  • Hot Flushes and/or Sweats
  • Hot Flushes, Menopause, Postmenopause
  • Night Sweats
  • Vasomotor Symptoms
  • Vasomotor Symptoms (VMS)
  • Vasomotor Symptoms Associated With Menopause

Eligibility Criteria

Sex
FEMALE
Age
40 Years - 70 Years
Healthy Volunteers
Not accepted

Interventions

  • JDS-HF3.0 — DIETARY_SUPPLEMENT
    Active Supplement JDS-HF3.0

Study Details

The goal of this study is to evaluate the efficacy of a neurokinin 1,3 antagonist on improving vasomotor symptoms (VMS) and overall menopause symptoms in women between the ages of 40-70. The primary research question is whether taking the study product daily for 4 weeks with an optional 8 week extension, significantly reduces the severity and frequency of menopause-related symptoms.

Key Dates

Start date
May 24, 2024
Status verified
Feb 2026
Primary completion
Dec 18, 2024
Completion
Dec 18, 2024

Study Design

Enrollment
112 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Active: JDS-HF3.0 Active Group
    All participants supplementing with JDS-HF3.0

Primary Outcome Measure

Change from Baseline on Hot Flash Symptoms assessed by the number and severity of hot flashes and times awakened at night due to night sweats collected via participant diary tracking electronically. [ Time Frame: From enrollment to initial end of study at 8 weeks and/or end of study at optional 12 weeks ]

Locations (1)

FacilityCityStateZIPSite coordinators
Bonafide HealthHarrisonNew York10528-

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