New Port Richey, FLNCT07834463Now EnrollingIRB Ready

Menopause Clinical Trial in New Port Richey, FL

Access cutting-edge menopause treatment through this clinical trial at a research site in New Port Richey. Study-provided care at no cost to qualified participants.

Sponsored by India Glycols Ltd

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Expert Care in New Port Richey

Access menopause specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related menopause treatment provided free

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Check if you qualify for this menopause clinical trial in New Port Richey, FL

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to New Port Richey

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit New Port Richey site if eligible
  4. 4Begin participation

About This Menopause Study in New Port Richey

This study will evaluate whether an 8-week course of a standardized herbal extract containing Shatavari and natural bio-enhancer ingredients can reduce menopausal symptoms in post-menopausal women. The study will compare the herbal extract with a matching placebo. Approximately 100 women aged 45 to 60 years with menopausal symptoms will be enrolled, with approximately 80 expected to complete the study. Participants will take one study product daily for 8 weeks. Menopausal symptoms, including hot flashes, mood, sleep, skin health, and hair and scalp health, will be assessed using questionnaires, a daily hot flash diary, blood tests, and safety assessments.

Sponsor: India Glycols Ltd

Who Can Participate

Inclusion Criteria

Female subjects aged 45-60 years at screening.
Post-menopausal status, defined as no menstrual period for at least 12 months, graded as post-menopausal per STRAW classification (not due to pregnancy, lactation, or medical/surgical causes).
Menopause Rating Scale (MRS) score \> 9 at screening.
Average frequency of hot flashes \>= 3 per day for at least 7 consecutive days prior to screening.
Willing and able to provide written informed consent and comply with study procedures, including maintaining the daily hot-flash diary.

Exclusion Criteria

Body mass index (BMI) \<= 18 kg/m2 or \> 35 kg/m2.
History of endometrial hyperplasia, endometrial cancer, cervical cancer, breast cancer, or other sex hormone-related cancers.
History of uterine resection or hysterectomy.
Unexplained abnormal uterine bleeding occurring after \>= 1 year of menopause.
History of severe migraine, or diagnosis of thromboembolism, cerebrovascular disease, myocardial infarction, unstable angina, or history of coronary angioplasty within 1 year prior to screening.
Currently undergoing treatment for severe disease of the cardiovascular, immune, respiratory, gastrointestinal/hepatobiliary, renal/urologic, nervous, or musculoskeletal system, or for infectious disease or malignancy.
Psychiatric disorders: clinically diagnosed depression, anxiety disorder, or sleep disorder within 3 months prior to screening treated with medication, or current use of neuropsychiatric drugs.
Use of thyroid hormones, clonidine, anticoagulants, antiplatelet agents (e.g., warfarin, clopidogrel), or osteoporosis treatments within 3 months prior to screening.
Use of any medication or plant-based hormone-like extract for menopausal symptoms within 3 months prior to screening.
Continuous intake of health functional foods related to menopause or herbal medicine within 1 month prior to screening.
Uncontrolled hypertension (resting blood pressure \>= 160/100 mmHg after 10 minutes of rest).
Uncontrolled diabetes (fasting blood glucose \>= 180 mg/dL or HbA1c \> 9.5%).
Excessive use of tobacco (\>20 cigarettes/day), caffeine (\>5 cups/day), or alcohol (\>14 drinks/week) within 4 weeks prior to screening.
History of clinically reported drug abuse within 1 year prior to screening.
Known clinically significant hypersensitivity to any component or excipient of the investigational product.
Participation in another interventional clinical trial within 1 month prior to study start.
Any other condition that, in the investigator's judgment, makes the subject unsuitable for participation.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in New Port Richey?

Yes, this clinical trial (NCT07834463) has an active research site in New Port Richey, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Menopause Treatment Options in New Port Richey, FL

If you're searching for menopause treatment options in New Port Richey, FL, this clinical trial (NCT07834463) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our New Port Richey research site is actively enrolling participants for this clinical trial. You'll receive care from experienced menopause specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all menopause clinical trials near you to find additional studies recruiting in your area.

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