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Our clinics will be close early on Tuesday, December 24th at 7pm and will remain closed on Wednesday, December 25th for the Christmas holiday.  All clinics will resume normal business hours on December 26th.  Wishing you and yours a very happy and healthy holiday season.  We look forward to caring for you!

Next Level
clinical research
studies
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RSV Study
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If you have recently tested positive for RSV, this research study may be for you! Must be 18 years of age or older to participate in the study.

Brain

Alzheimer's Study
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If you are between the ages of 55 and 80 and would like to know whether you are positive for the Alzheimer’s biomarker, this study, measuring the effectiveness of Alzheimer’s treatment, may be a good fit for you. 

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Obesity study - Nov 2024

If you’re 18 years of age or older with a BMI of 35+, you may qualify to participate in our study! Pre-screenings are now being conducted.

scales

Obesity study - Nov 2024

If you’re 18 years of age or older with a BMI of 35+, you may qualify to participate in our study! Pre-screenings are now being conducted.

lungs

Lung cancer screening study

Are you an avid smoker who is 50 years of age or older? You may qualify to participate in our lung cancer screening study!

lungs

Lung cancer screening study

Are you an avid smoker who is 50 years of age or older? You may qualify to participate in our lung cancer screening study!

The Next Level experience - our mission

We are committed to providing the highest standard of agility, quality results oriented data, and participant care. With a combined experience of over 20 years in clinical research; our dedicated staff of principal investigators are board certified physicians with all applicable certifications such as GCP. Our clinical coordinators hold certifications in HIPPA, GCP and IATA with advanced degrees in areas of BSN-registered nurse, biology, clinical research, and organizational management. 

Why participate in clinical trials?

It is healthcare heroes like you who make new treatments possible. By participating in a clinical trial, you may benefit from new investigational treatments that are not otherwise available to the public. As a participant in a clinical trial, no health insurance is required. You will receive free medical care from expert physicians and all study-related medical exams, laboratory tests, and procedures are provided at no charge. 

A clinical trial is medical research to study the safety and effectiveness of an investigational drug or device. The US Food and Drug Administration (FDA) uses information gathered in clinical trials to evaluate medications before approving them for use in the United States.

Before you are evaluated as a research participant, we will provide you with an approved Informed Consent Form (ICF) which you must read, understand, and sign before enrolling. The ICF outlines all procedures you will need to go through and all known risks and side effects of the investigational medication. Please read it carefully and ask all questions you might have.

Before conducting a clinical trial, pharmaceutical companies must obtain approval from the FDA to ensure that the investigational medication is appropriate to give to people. Additionally, all study procedures are reviewed by an independent Investigational Review Board (IRB) before they are allowed to be administered. All this is done to ensure that the study is ethical and that the risks are as low as possible. However, since the study participants are among the first to try the investigational medication, the risk of unanticipated side effects does exist. This is why the health of the people participating in the trials is continuously monitored and any serious side effects experienced by any of the people in the trial are promptly investigated.  If necessary, corrective actions, including termination of the trial, are taken.

Different studies have different enrollment requirements. Some studies are open only to healthy adults, while others look for people with specific medical conditions. To determine whether you can enroll, we will ask several questions about your current health, your medical condition, and the medications you are taking. If you meet the study requirements, an appointment will be scheduled for you to be evaluated in person.

Your participation in a research study is entirely voluntary, and you may withdraw from participation at any time and for any reason. During your screening visit and throughout the study, we will fully explain the risks and benefits of your study. If you change your mind, you may withdraw.

Any information you provide as a research participant is strictly confidential. It will not be sold and will be used only for the purposes of contacting you for relevant research studies.

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