Menopause-Hot Flashes

7

Review clinical trials related to Menopause-Hot Flashes. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Effect of Tirzepatide on Menopausal Vasomotor Symptoms and Biological Aging in Post-menopausal Women With Obesity

The purpose of this study is to determine the effect of tirzepatide on vasomotor symptoms and on measures of biological aging.

Participants needed: 40
Trial details
Phase: Phase 4Age: 46-60Biological sex: FemaleType: InterventionalSponsor: Mayo ClinicUpdated: Oct 6, 2026Locations: 1
Eligibility criteria

Females [+7]

Current or recent use (past 4 weeks) treatment with menopausal hormone therapy. [+16]

Status: Recruiting

Effects of a Dietary Intervention Based on the Dietary Guidelines for the Brazilian Population on the Reduction of Menopausal Symptoms in Overweight and Obese Women

The menopausal transition is associated with significant hormonal changes that negatively impact many women's quality of life. Vasomotor symptoms, sleep disturbances, mood changes, and genitourinary symptoms are frequently reported during this period. Concurrently, there is a tendency toward increased body weight and fat redistribution, specifically central fat accumulation, which raises the risk of metabolic diseases. Although hormonal therapy is effective, it is not suitable for all women, necessitating the consideration of non-pharmacological strategies as therapeutic alternatives. Scientific evidence indicates that healthy dietary patterns and weight loss are associated with reduced menopausal symptom severity. The objective of the research is to evaluate the effects of a dietary intervention based on the guidelines of the Dietary Guidelines for the Brazilian Population (GAPB) on the reduction of menopausal symptoms. A randomized clinical trial will be conducted to assess whether improving dietary quality and reducing body weight contribute to alleviating menopausal symptoms. Participants will be assigned to two groups: a control group (CG) and an intervention group (IG). Both groups will receive nutritional guidance based on the GAPB; however, the CG will receive the guidelines in printed format, whereas the IG will receive them through group sessions. The study will include perimenopausal or postmenopausal women who are overweight or obese and experiencing menopausal symptoms. Validated instruments will be administered at the beginning and end of the study to assess dietary patterns, menopausal symptoms, and nutritional status.

Participants needed: 74
Trial details
Age: 40-65Biological sex: FemaleType: InterventionalSponsor: Federal University of Health Science of Porto AlegreUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Aged 40 to 65 years [+5]

Pregnancy [+4]

Status: Recruiting

Thermoregulatory Physiology of Menopausal Hot Flashes

This study is evaluating the effects of cooling on menopausal hot flashes in midlife women. Precise targeted cooling is provided to areas of the skin when a hot flash occurs.

Participants needed: 40
Trial details
Age: 40-65Biological sex: FemaleType: InterventionalSponsor: SRI InternationalUpdated: Sep 17, 2026Locations: 1
Eligibility criteria

Female [+3]

History of medical or neurological illness or trauma that would affect the centr... [+4]

Status: Recruiting

Haelan 951 for Menopause Symptoms in Peri- and Postmenopausal Women

This proof-of-concept, open-label, single-arm study is designed to evaluate the effects of daily consumption of Haelan 951, a fermented soy conventional food product, on self-reported menopausal vasomotor symptoms, sleep quality, and health-related quality of life in peri- and postmenopausal women. The study will collect descriptive data on participant-reported outcomes over the study period to assess the feasibility and potential effects of Haelan 951 in supporting menopausal wellness. The study is not intended to evaluate the treatment, prevention, or cure of any disease.

Participants needed: 25
Trial details
Age: 45-65Biological sex: FemaleType: InterventionalSponsor: Spectrum Clinical Research, LLCUpdated: Sep 11, 2026Locations: 1
Eligibility criteria

Female sex assigned at birth, ages 45-65 years inclusive at the time of consent. [+8]

Pre-menopausal status (STRAW+10 stage -3 or earlier). [+12]

Status: Not yet recruiting

Fezolinetant and Vascular Health and Brain Health

The goal of this clinical trial is to learn whether a study drug called fezolinetant impacts cardiovascular and cognitive health in women who have moderate to severe menopausal hot flashes and night sweats. Researchers will compare fezolinetant to a placebo. A placebo is a pill that looks like the study drug but does not contain any active medicine. This comparison helps researchers understand whether fezolinetant works better than no treatment. Participants will: Be randomly assigned to take either fezolinetant (45 mg) or a placebo once a day for 12 weeks. Visit the research clinic for regular checkups and tests during the study. Complete tests that measure blood vessel function and cognition. Participants and study staff will not know which treatment each participant receives during the study.

Participants needed: 220
Trial details
Phase: Phase 3Age: 40-65Biological sex: FemaleType: InterventionalSponsor: Rebecca ThurstonUpdated: Aug 19, 2026Locations: 2
Eligibility criteria

Born female [+7]

Pregnancy/lactation (past 6 months) [+20]

Status: Recruiting

Focusing on the Menopausal Transition to Improve Mid-Life Women's Health

What if midlife women, who are inherently at an increased risk for future cardiometabolic disease due to transitioning into menopause, had access to a suite of evidence-based health interventions? Could these interventions reduce menopause-related inflammation, restore a healthier cardiometabolic profile, reverse epigenetic aging, and reduce bothersome menopausal symptoms? The ultimate goal of this work is to attenuate future disease and enhance women's quality of life, extend healthspan and increase productivity.

Participants needed: 200
Trial details
Phase: Phase 2, Phase 3Age: 45-55Biological sex: FemaleType: InterventionalSponsor: University of Colorado, DenverUpdated: Jul 21, 2026Locations: 3
Eligibility criteria

aged 45-55 [+4]

Lack of broadband access (activity and survey data will be collected electronica... [+6]

Status: Not yet recruiting

Transcranial Electrical Stimulation for Noninvasive Study of Menopausal/Perimenopausal Symptoms

Participants are being invited to a research study. This research aims to assess the tolerability of transcranial electrical stimulation of the brain, and explore the response of TES on menopausal/perimenopausal symptoms including hot flashes effects, depression/anxiety, memory-problems, and muscular problems. This study will assess what types of electrical brain stimulation affect different menopausal related symptoms. This study will help guide the development of electrical stimulation to be used for improving women's health during menopause transition.

Participants needed: 50
Trial details
Age: 40-60Biological sex: FemaleType: InterventionalSponsor: Carnegie Mellon UniversityUpdated: Jan 29, 2026
Eligibility criteria

Age between 40 and 60 years [+6]

Disorders that may mask or coincide with menopause and peri-menopause, such as:... [+3]