Omaha, Nebraska
- (402) 934-0044
- 10040 Regency Circle, Suite #375, Omaha, Nebraska 68114
Select Your Study of Interest
Be The Miracle
The Future of Health Begins With You
- Access to New Treatments
- Medical Exams at no cost
- Receive Compensation
Participating
What are the
Benefits of Participating
Receive Compensation
Qualified participants will be compensated for study related efforts.
Access to
New Treatments
Receive therapies that are not yet available to the general public.
No-Cost Exams
& Appointments
Exams for qualification in studies are provided at no cost to the patient.
Specialized Care at No-Cost
Participants receive
no-cost care from experienced physicians.
Making a Difference
You'll play an active role in improving future patient care outcomes.
No Insurance
Required
Medical insurance is not required to participate in our clinical trials.
What to Expect as a Clinical Trial Participant
- Click an Arrow to Learn More
Before joining a clinical trial, you will go through the informed consent process. This involves receiving detailed information about the trial, including its purpose, potential risks and benefits, procedures involved, and your rights as a participant. You will have the opportunity to ask questions and fully understand what participation entails.
To ensure the trial’s objectives are met and participant safety is maintained, you will undergo a screening process. This typically involves a series of assessments, including medical history review, physical examinations, laboratory tests, and sometimes imaging scans. These evaluations help determine if you meet the specific eligibility criteria for the trial, which may include factors such as age, medical condition, previous treatments, and overall health.
If you qualify for the clinical trial and choose to participate, you will receive the investigational treatment or intervention being studied at no-cost. This may involve a new drug, medical device, procedure, behavioral intervention, or a combination of treatments. In some cases, you may be assigned to a control group receiving a placebo or standard treatment for comparison purposes. The specific details of the treatment plan, including dosages, frequency, and duration, will be explained to you by the research team.
Throughout the trial, you will be closely monitored by the research team. This may include regular visits to the study site or interactions via telemedicine, depending on the trial design. The team will assess your progress, monitor any potential side effects, and evaluate the treatment’s effectiveness. You may need to undergo additional tests, procedures, or imaging scans during the trial to gather data and track your response to the intervention.
To ensure the integrity and validity of the clinical trial results, it is important to follow the study protocol diligently. This includes adhering to the treatment schedule, taking medications as prescribed, attending scheduled appointments, and reporting any changes in your health or potential side effects to the research team. It’s crucial to communicate openly with the research staff and notify them of any concerns or questions that arise during the trial.
Your safety and well-being are of utmost importance throughout the clinical trial. The research team will have safety measures in place to monitor and manage any potential risks or adverse events. They will provide guidance on how to handle emergency situations and offer support throughout the trial duration. It’s essential to promptly report any unexpected changes in your health or any adverse reactions you experience during the trial.
Participation in a clinical trial is completely voluntary. You have the right to withdraw from the trial at any time for any reason.
As a participant in a clinical trial, you may be entitled to compensation and travel-related reimbursement for your efforts and involvement. Patients will receive stipends after each visit or phone call in the study. Receiving compensation does not change your right to leave the study at any time. You will still be compensated for the portion you completed up to that point, if applicable.
You can expect ongoing communication with the research team during the trial. They will provide updates on the trial progress, address any concerns or questions you may have, and ensure that you remain informed about your participation. Additionally, they will inform you about any changes to the study procedures, interventions, or potential risks as they arise.
The investigational treatment, study-related tests, and medical visits are provided at no cost. If unexpected health issues arise directly from the study, the trial may cover those costs as well.
Our Team
Meet Our Clinic Staff
Dr. Brian Hollis
- MD, CPI, Internal Medicine
Jennifer Larsen
- Clinical Research Coordinator
- BS, RT (R)(BD)(ARRT), CDT, CCRC
Dr. John Peters
- MD, Opthalmology
Danielle Butler
- Quality Control Specialist



