Trial · Interventional
RecruitingPhase 4Registry dataThe Effect of Tirzepatide on Menopausal Vasomotor Symptoms and Biological Aging in Post-menopausal Women With Obesity
Overview
- Status
- Recruiting
- Phase
- Phase 4
- Enrollment
- 40 participants (estimated)
- Sponsor
- Mayo Clinic · Other
- Design
- Randomized · Quadruple masking
- Countries
1 country
United States
- Start
- 8 Apr 2026
- Primary completion
- 18 Sept 2027 (estimated)
- Completion
- 18 Sept 2027 (estimated)
- First posted
- 20 Oct 2025
- Last update posted
- 6 Oct 2026
- Conditions
- Obesity · Menopause Hot Flashes
Timeline
1 trial · 1 ongoing
- Completed
- Ongoing
- Not yet recruiting
- Stopped
- Estimated dates (est.)
- Results posted
- Ph 4
The Effect of Tirzepatide on Menopausal Vasomotor Symptoms and Biological Aging in Post-menopausal Women With Obesity
NCT072184458 Apr 2026 to est. 18 Sept 2027
Registry summary
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
The purpose of this study is to determine the effect of tirzepatide on vasomotor symptoms and on measures of biological aging.
Interventions
- TirzepatideDrug
- PlaceboDrug
Arms2
Experimental
Tirzepatide
Participants will receive tirzepatide for 24 weeks, in addition to standard lifestyle modification recommendations
Placebo comparator
Placebo
Participants will receive a placebo for 24 weeks, in addition to standard lifestyle modification recommendations
Primary outcomes4
Outcomes the sponsor listed as primary.
Change in Vasomotor Symptoms Frequency
Time frame · Baseline, 24 weeks
Registry description
Change in the frequency of self-reported daily average vasomotor symptoms from baseline to 24 weeks. Vasomotor symptoms will be captured for 2 weeks at baseline and 2 weeks at the end of the study.
Change in Vasomotor Symptom Severity
Time frame · Baseline, 24 weeks
Registry description
Change in self-reported daily vasomotor symptom severity from baseline to 24 weeks. Vasomotor symptoms will be captured for 2 weeks at baseline and at the end of the study. Severity will be classified as follows: Mild, sensation of heat without sweating/dampness; Moderate: sensation of heat with sweating/dampness, but able to continue current activity. May briefly fan yourself; Severe: sensation of intense heat with sweating causing disruption of current activity.
Aging Biomarkers: Cellular Senescence Markers in Plasma
Time frame · 24 weeks
Registry description
Cellular senescence markers are measured in plasma samples to assess biological aging and cellular stress. These markers may include proteins associated with the senescence-associated secretory phenotype (SASP). Quantification is performed using immunoassays. Higher levels of senescence markers indicate increased cellular senescence.
Difference between biological and chronological age
Time frame · 24 weeks
Registry description
Epigenetic clocks estimate biological age by analyzing DNA methylation patterns at specific CpG sites across the genome. Biological age estimates are compared to chronological age to assess aging acceleration or deceleration. Biological age greater than chronological age indicates accelerated biological aging and potential increased risk of morbidity and mortality. Primary measure is the difference (ΔAge) between biological and chronological ages = reported in years.
Secondary outcomes(14)
Change in Reactive hyperemic index
Time frame · Baseline, 12 weeks and 24 weeks
Registry description
Vascular function will be measured using the EndoPAT device to assesses reactive hyperemia index (RHI) from baseline to week 24 on treatment or placebo. RHI is automatically calculated through a computer algorithm by following the equation: \[(tested arm-post occlusion/tested arm-baseline)/(control arm-post occlusion/control arm-baseline)\] × baseline correction factor. Endothelial dysfunction is defined as having an RHI ratio of equal or less than 1.67.
Change in Augmentation Index percentage
Time frame · Baseline, 12 weeks, and 24 weeks
Registry description
Augmentation Index (AIx): AIX uses applanation tonometry of the radial artery pulse, calibrated to resting brachial systolic and diastolic pressures (SphygmoCor XCEL, Medtronic, Minneapolis, MN). Aortic systolic, diastolic, and pulse pressures will be derived from a synthesized aortic waveform using a validated mathematical transfer function. Augmentation pressure, reflecting the difference between aortic systolic pressure and the inflection point caused by the reflected wave, is influenced by arterial stiffness as well as factors like heart rate and ejection dynamics. AIx is calculated as augmentation pressure divided by aortic pulse pressure × 100%, adjusted to a heart rate of 75 bpm (AIx@75 bpm). Measurements will be performed in duplicate and averaged.
Change in Pulse Wave Velocity
Time frame · Baseline, 12 weeks, and 24 weeks
Registry description
SphygmoCor estimates central arterial stiffness by calculating the speed at which the pressure wave travels between the carotid and femoral arteries using applanation tonometry and reported as the pulse wave velocity (PWV); PWV m/s
Change in Cardiometabolic Parameters: Blood Pressure
Time frame · Baseline, 24 weeks
Registry description
Change in cardiometabolic parameters including blood pressure from baseline to week 24 on treatment or placebo. Measured in mmhg
Change in Cardiometabolic Parameters: Fasting Glucose
Time frame · Baseline, 24 weeks
Registry description
Change in cardiometabolic parameters including fasting glucose from baseline to week 24 on treatment or placebo. Measured in mg/dL
Changes in Cardiometabolic Parameters: HbA1C
Time frame · Baseline, 24 weeks
Registry description
Change in cardiometabolic parameters including HbA1C from baseline to week 24 on treatment or placebo. Measured in %
Changes in Cardiometabolic Parameters: Lipoprotein profile
Time frame · Baseline, 24 weeks
Registry description
Change in cardiometabolic parameters including Lipoprotein profile from baseline to week 24 on treatment or placebo. Measured in mg/dL
Changes in Cardiometabolic Parameters: hsCRP
Time frame · Baseline, 24 weeks
Registry description
Change in cardiometabolic parameters including hsCRP from baseline to week 24 on treatment or placebo. Measured in mg/L
Change in Physical Function Measure: Short Physical Performance Battery (SPPB) score.
Time frame · Baseline, 24 weeks
Registry description
The SPPB is a standardized test that evaluates lower extremity function using three components: balance tests (standing in various positions), gait speed (walking a short distance), and chair stand (repeated standing from a seated position). Each component is scored from 0 to 4; the total score ranges from 0 to 12. Higher scores represent better physical function
Change in Physical Function Measure: Modified Clinical Test of Sensory Interaction in Balance (mCTSIB) performed on the Rehabilitation Artificial Physical Intelligence Database (RAPID) foot pressure mat
Time frame · Baseline, 24 weeks
Registry description
The mCTSIB assesses balance under four sensory conditions: eyes open/closed on firm and foam surfaces. Testing is performed while standing on the RAPID foot pressure mat, which captures center of pressure and postural sway data. The primary measure is average sway area of the four sensory conditions. The sway area is the area which is required to correct equilibrium, representing the total area covered by postural sway, measured in square centimeters (cm²).
Change in Physical Function Measure: Standing Chest Throw Test with a 2-kg Weighted Ball using Motion Sensor Technology (MST)
Time frame · Baseline, 24 weeks
Registry description
This test evaluates upper body muscular power. Participants perform a two-handed chest throw of a 2-kg medicine ball from a standing position. The MST is used to record throw distance, velocity, and related performance metrics. The primary measure is Peak Power Score (W).
Change in Physical Function Measure: Chair-to-Stand Tests using Motion Sensor Technology (MST)
Time frame · Baseline, 24 weeks
Registry description
This test assesses lower body strength and function. Participants are instructed to stand up from a chair and sit back down five times without using their arms. The MST measures movement dynamics. The primary measure is peak power score (W).
Change in Physical Function Measure: Six-Minute Walk Test (6MWT)
Time frame · Baseline, 24 weeks
Registry description
The 6MWT is a standardized submaximal exercise test used to assess functional aerobic capacity. Participants are instructed to walk as far as possible in six minutes along a flat, straight course. The total distance walked is recorded in feet. Longer walking distances indicate better aerobic capacity and endurance.
Change in Physical Function Measure: Hand Grip Strength using a Hydraulic Hand Dynamometer
Time frame · Baseline, 24 weeks
Registry description
Participants are instructed to squeeze the dynamometer with maximum effort, measured in kilograms. The highest value from multiple trials is recorded.
Posted results
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
No results are posted for this trial.
A trial that is still running, or that stopped early, may post results later.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies0
Studies that cite this trial.
No study cites this trial.
Eligibility
Who could join, as posted.
- Sex
- Female
- Age
- from 46 Years up to 60 Years
- Healthy volunteers
- Accepted
Inclusion and exclusion criteria, as posted
PepBank is a research reference. Talk to a doctor before you use any peptide.