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614-501-6164

Paid Clinical Trials and Medical Research Studies
in Columbus OH, Phoenix AZ, and Erie PA

Current Studies for Women's Health

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Special clinical studies designed to bring medical advancements and opportunities to women in Central Ohio. From contraceptives to menopausal treatment alternatives, we have a variety of studies open and available to you.

Below are listed the current studies we are conducting. If you are interested in finding out more or taking part in one of these clinical trials, use the contact form or call us.

We are actively recruiting patients for the following trials:

Breast Density Clinical Trials

Breast density is ONLY detectable on mammogram. Dense breast tissue occurs in breasts that have more connective tissue than fatty tissue. Breast density appears white on mammograms.

Because breast cancers also appear white on mammograms, having more breast density can obscure the appearance of any cancers. In addition, the presence of more breast density is actually linked to an increased risk of developing breast cancer.

HOW DO I KNOW IF I HAVE BREAST DENSITY?

Density seen on mammograms is graded by the radiologist on a scale of A to D. Doctors are now required in 36 states, including Ohio, to notify patients when density is seen.

WHAT CAN BE DONE ABOUT BREAST DENSITY?

If breasts appear significantly dense on mammogram, extra testing can be done such as 3D mammogram, ultrasound, or MRIs.

At Aventiv Research we are currently investigating a novel treatment for breast density. Please contact us if you are interested in enrolling by calling 614-501-6164 or completing our volunteer form.

Sign Up for Clinical Trial

Hypoactive Sexual Desire Disorder

Hypoactive sexual desire disorder is a sexual dysfunction in which individuals either have low or non-existent sexual desire. This condition can be acquired or be lifelong.

If you suffer from hypoactive sexual desire disorder or inhibited sexual desire, you may qualify for a clinical trial. Many experimental medications are being tested now that may boost sexual desire in women. By participating in a clinical trial, you gain access to medication before it is generally available.

Aventiv Research is currently researching a hyposexual desire disorder medication. If you qualify, you will receive all the necessary examinations, lab work and medication at no cost. You may also be compensated for your time and travel.

Sign Up for Clinical Trial

Birth Control Patch

Are you interested in a research study of a new investigational birth control patch? If you are:

  • Sexually active and willing to try a different method of birth control; or
  • Interested in being in a study for a method of birth control that is non-invasive,

Then you may be eligible to join the SECURE Study-a clinical study of a new birth control patch.

We are recruiting women to join a large clinical research study of a contraceptive patch. The patch contains the same type of hormones that are in many birth control pills. The patch is designed to be flexible and and is applied onto the skin, just once a week.

To join the study you must:

  • Be sexually active at least once a month
  • Need to use birth control
  • Not wish to become pregnant for at least 1 year
  • Be able to use the patch as your only form of birth control for at least 1 year.

Not everyone who wants to join will be able to. Several joining criteria must also be met. It is your choice whether to join, and even if you do join, you can leave the study at any time.

Contraceptive patches and all study check-ups will be provided at no cost to you.

Sign Up for Clinical Trial

Hot Flashes

If you are a woman between the ages of 40 and 65, and are suffering from hot flashes and sweating due to menopause, you are invited to see if you may qualify for the REPLENISH Trial. The purpose of this research study is to evaluate the safety and effectiveness of an investigational medication for menopause associated hot flashes and sweating.

Each individual will be evaluated to determine her eligibility to participate in this study. If you qualify, you will receive investigational medication, study-related exams, and laboratory services at no charge. You may also be reimbursed for time and travel and other expenses.

In order to participate in the trial, women must be evaluated by a trial doctor and meet certain requirements including:

  • Being a female between the ages of 40 and 65
  • Being postmenopausal with an intact uterus
  • Be in generally good health
  • Be willing to particiapte in a clinical trial

Sign Up for Clinical Trial

Vaginal Atrophy

You may be eligible to participate in a clinical trial testing an investigational vaginal treatment for vaginal atrophy in women surgically or naturally in menopause.

Qualified participants must: be a healthy postmenopausal woman between the ages of 30 and 75, bothered by one of the following symptoms: vaginal dryness, vaginal or vulvar irritation or itching, or pain associated with sexual activity, and not currently on hormone therapy.

Participants may receive: study related exams, study-related medication, compensation for time and travel

Sign Up for Clinical Trial

Overactive Bladder

Do you have an overactive bladder? If so, you could be eligible to participate in our clinical trial on the condition.

Qualified participants must: Be a woman over the age of 18, who suffers from overactive bladder (OAB). This condition causes you to experience a sudden urge to urinate that you cannot control, and sometimes even causes leaking urine. Another symptom of OAB is the need to go to the bathroom many times during both day and night.

Participants may receive: study-related exams, medication, and/or physical therapy, and compensation for time and travel.

Sign Up for Clinical Trial

What Our Clients say

  • The staff is all extremely friendly and professional. Looking forward to future studies

    P. Oakley
  • This is a great way to make extra money and be involved in a research study that will help and benefit many people to come. Thanks. I’ve really enjoyed myself with the program and with the staff.

    V. Ivory
  • Have found a significant change to the better from my research study. I experienced less shortage of breath and much better sleep. My daily activities are less hampered because of my better breathing. Thank you all.

    J. Drasko, Jr.
  • Excellent staff. Dr. Arora took the time to not only explain everything but made every step of the research process a very pleasant, hopeful and informative journey.

    BDT

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