Clinical Research

Studies

FAQ

Staff

Dr. Janet Gersten started New Age Medical Research Corporation in 2000. We have completed over 100 major clinical trials and have generated numerous publications under Dr. Gersten’s direction. New Age Medical Research Corporation specializes in clinical trials related to women’s health and general medicine. Four full-time board-certified doctors currently oversee all studies at New Age Medical Research. These doctors do not create or manufacture drugs. Instead, they act as a neutral third party who tests the drugs that someone else has manufactured. These studies are all highly regulated and New Age Medical Research is subject to random audits by the Food and Drug Administration (FDA).

Studies

Stress Urinary Incontinence

New Age Medical Research will be assessing the effect of an investigational oral weight loss medication in women with urinary incontinence. Participants for this study must have a history of leaking urine with coughing, sneezing, laughing, exercising, etc. This study will last approximately one year. All study-related care and lab tests will be provided at no cost and no health insurance is required. Participants have an opportunity to receive compensation for their participation.

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Birth Control Patch

New Age Medical Research is currently enrolling women in an investigational birth control patch clinical research study. The study will last approximately 13 months. All study-related care and lab tests will be provided at no cost and no health insurance is required. Participants have an opportunity to receive compensation for their participation.

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FAQ

A clinical trial is a medical research study involving human subjects. They are often designed to test new medications or treatments. Clinical trials are completely voluntary to join and can be stopped at any time for any reason. You can only join a clinical trial if you meet certain requirements or qualifications.

Technically, there are four different types of clinical trials performed in humans: Phase I, Phase II, Phase III, and Phase IV. Phase I studies test whether or not a new drug is safe and to identify side effects. These studies are only done on a small number of people, typically under 100. Phase II studies are done to determine drug dosing and efficacy in an attempt to figure out how well the medication works. Phase III studies are done on larger groups of people (usually in the thousands) and determine efficacy, effectiveness, and further monitor side effects. Often several Phase III studies need to be performed for a drug to be approved by the Food and Drug Administration (FDA). Phase IV studies are then done once a drug has been approved by the FDA to further track overall risks, benefits, and optimal use. It is important to note that all drugs must start at Phase I and successfully pass each phase before being approved for the next.

New Age Medical Research Corporation performs Phase II, Phase III, and Phase IV trials.

Clinical trials help to discover new medications or treatments for all types of diseases and disorders. They also can improve or advance the development of medicines or treatments that already exist. Your participation in a trial will make a difference in the fields of women’s health and general medicine.

Participants are also paid for their time and travel expenses while participating, typically ranging from $25-$200 per visit (varies per study). Study visits are performed on-site in our office. Some testing may be done at other local facilities. Clinical trials often provide participants with physical examinations, bloodwork, Pap smears, STI tests, ultrasounds, and mammograms at no cost.

It does not cost anything to participate in a clinical trial. Instead, you are often paid for your time and efforts, ranging anywhere from $25-$200 per visit but the exact amount varies per study. All testing that is part of the study (visits with a doctor, physical examination, blood tests, pap smears, EKGs, ultrasounds, mammograms, etc) are provided for free.

No, you do not need health insurance to join a clinical trial. We do not involve your medical insurance company during your time in a clinical trial.

Each clinical trial is unique and has specific requirements participants must meet in order to join. The best way to see if you qualify is to call our office and speak with us about it directly. You can also apply online and one of our staff members will reach out to you.

You are typically compensated when you are involved in a clinical trial, ranging anywhere from $25-$200 per visit but the exact amount varies per study.

Being in a clinical trial is completely voluntary. You can stop a study at any time for any reason.

Clinical trials generally last anywhere from several months to several years. We also do one-time specimen collections where only one test such as one blood draw, a single urine sample, etc is needed. You receive compensation for these samples as well, usually anywhere from $25-$100.

When you are part of a clinical trial, all medical care given is based upon a specific study protocol. For example, each visit that is part of a study may involve certain tests such as urine tests, blood work, a physical exam, etc., regardless of whether or not you are experiencing symptoms.

Yes, we can add you to our contact list. Please either call our research office at 305-596-9901 or submit your information HERE

Are you ready to participate in our clinical research?

Would you like to be added to our contact list to be notified about future studies?

Staff

Joanna Bedell
MD, FACOG

Sarah Bedell
MD, FACOG

Victoria Bedell
MD, FACOG

Janet Gersten
MD, FACOG

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    Study Types:

    Intrauterine Device (IUD)Weight LossGenerally Healthy Patient StudiesGeneral InformationBirth ControlVaccinesSingle blood draw studiesDermatologyObesityType 2 DiabetesUrinary Incontinence