Frequently Asked Questions
Most FAQ's About Clinical Trials
fAQ's
What is a clinical trial?
A clinical trial are research studies conducted by medical professionals to see the effects of certain drugs have on a particular population. At Health Research of Oklahoma, we know that science is constantly evolving and new drug compounds and treatment options become available through thorough research. We collaborate with pharmaceutical companies to conduct ethical treatment for our study patients.
Drug development can take several years before it even reaches the clinical trial stage and there are 4 stages of clinical trials.
How are you protecting my personal information?
Research is completely confidential. Once enrolled in a study, you are assigned a subject number. Your name and personal information is not provided to anyone. No one will know that you are in a research study. All research trials conducted must be in compliance with HIPAA.
Can I quit the trial at any time?
Yes you can. Research is completely voluntary and is not legally binding. You can stop the study at any time.
What is the process?
To see if you qualify please call our office at 405-702-6770. We first speak to you over the phone to see we think you would be a good fit for a research study. We then schedule you for a screening visit.
At this visit you’ll be presented with the informed consent to read. You will be given plenty of time to ask questions and you will be given a signed copy to keep. You will see the study doctor, typically have your blood drawn as well as other assessments (questionnaires, ECGs, etc.) and your relevant medical history will be reviewed.
If you are able to move forward with the study then you will have what is called a baseline visit. This is typically the visit that you are provided study drug. You are officially enrolled in the trial and will be given plenty of training on how to use the medication and you will schedule your next research appointment.
Will I receive a bill for my participation?
You will never receive an invoice or bill for a research study.
Do I need insurance to participate?
You do not need insurance to participate.
What are the benefits and risks?
Benefits of Participating in a Clinical Trial
- Assessments associated with study treatment are provided at no cost to the participant.
- Study participants may have access to newer treatment options not currently available on the market.
- Study participants are monitored closely. Participants work closely with the research staff and are seen by the study doctor routinely for safety and efficacy.
- The study doctor is easily accessible if questions arise during the study.
- Contributing in research may help others in the future.
- Compensation is often provided for cost of travel.
- You are able to take a more active role in your health care.
Risks of Clinical Research
- The study treatment may not be beneficial to you
- The study treatment may cause side effects
- You could be assigned to the control group, meaning that you could be getting placebo
- The research study could require time for appointments, travel and may not coincide with your schedule.
For More Information Please Visit Clinicaltrials.gov
Or Call US at: 405-702-6770