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Hormone Therapy
Estradiol for Perimenopause
Phase 4
Recruiting
Research Sponsored by University of Delaware
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Live in Delaware
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to day 7
Awards & highlights
All Individual Drugs Already Approved
Approved for 5 Other Conditions
Drug Has Already Been Approved
Pivotal Trial
Summary
This trial studies how estradiol, a form of estrogen, affects blood vessel health in peri-menopausal women. The goal is to see if estradiol can improve the function of cells lining the blood vessels, potentially reducing the risk of cardiovascular disease. Estradiol has been shown to reduce cardiovascular disease by direct and indirect effects on the cardiovascular system, with recent evidence suggesting beneficial actions of its metabolites.
Who is the study for?
This trial is for peri-menopausal women aged 40-58 living in Delaware, experiencing changes in their menstrual cycles or short-term amenorrhea. It's not open to those with cardiovascular disease, blood clots, stroke, cancer, liver disease, extreme body weights (BMI <18 or >30), tobacco users, pregnant/breastfeeding women, high blood pressure patients not controlled without medication.
What is being tested?
The study tests the effects of Estradiol patches on vascular endothelial function in peri-menopausal women. Participants will either receive the Estradiol patch or a placebo to compare outcomes and understand how advancing reproductive age affects vascular health.
What are the potential side effects?
While specific side effects are not listed here, typical ones associated with hormone treatments like Estradiol may include skin irritation at the patch site, headaches, breast tenderness/pain and nausea.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline to day 7
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to day 7
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Vascular Endothelial Function (Flow mediated dilation or FMD)
Secondary study objectives
Endothelial Cell Protein Expression
Endothelin Receptor Responses
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 5 Other Conditions
This treatment demonstrated efficacy for 5 other conditions.
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: EstradiolExperimental Treatment1 Intervention
Transdermal estradiol (0.1mg/day patch)
Group II: PlaceboPlacebo Group1 Intervention
Placebo
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Hormonal treatments for perimenopause, such as estradiol (E2), work primarily by supplementing declining estrogen levels, which helps alleviate symptoms like hot flashes, mood swings, and vaginal dryness. Estradiol, a form of estrogen, can improve vascular endothelial function, which is crucial for cardiovascular health.
This is particularly important for perimenopausal patients as they experience hormonal fluctuations that can lead to endothelial dysfunction, increasing the risk of cardiovascular diseases. By stabilizing estrogen levels, these treatments help maintain vascular health and overall well-being during the perimenopausal transition.
MPA and postmenopausal coronary artery atherosclerosis revisited.
MPA and postmenopausal coronary artery atherosclerosis revisited.
Find a Location
Who is running the clinical trial?
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,929 Previous Clinical Trials
47,765,147 Total Patients Enrolled
University of DelawareLead Sponsor
161 Previous Clinical Trials
25,562 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Live in DelawareI have a history of heart disease, blood clots, stroke, cancer, or liver disease.I am a woman with high blood pressure, diagnosed or on medication.I am allergic to latex.I am a woman aged 40-58 experiencing irregular periods or a pause in my menstrual cycle.I use tobacco products.I am a woman who has had a hysterectomy or used hormones in the last 3 months.I am a woman with a neurological disease or diabetes.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo
- Group 2: Estradiol
Awards:
This trial has 4 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- Approved for 5 Other Conditions - This treatment demonstrated efficacy for 5 other conditions.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Perimenopause Patient Testimony for trial: Trial Name: NCT04255160 — Phase 4
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