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PLEASE FIND RESEARCH STUDIES AVAILABLE FOR OUR CLINIC IN PALMETTO BAY
Females aged 18 and above who:
Are you taking a high sodium oxybate medicine like Xyrem? If so, we are enrolling
Narcolepsy Study
Age Range 18-70 years old
Compensation Up to $1200
First, sign up with your email address and fill out a questionnaire to find out whether you pre-qualify for the study. If you are a match and want to participate, you will need to fill out a Medical Release Consent Form so we may confirm your Narcolepsy diagnosis with your healthcare provider(s). We will then walk you through the steps of enrollment and informed consent process.
The study duration for each participant will be up to approximately 11 weeks. Participants will attend up to 8 virtual visits. This study will be done virtually, which means we will come to you to do the study assessments. The study doctor will be available through telemedicine and a mobile research team member will come to your home. We will need to evaluate you to see if you qualify for the study. This evaluation is at no cost to you, and will include a collection of vitals and an electrocardiogram (ECG).
If qualified, you can take part in a research study evaluating blood pressure changes in narcolepsy participants when switching from high-sodium oxybate to a low-sodium oxybate.
Are you interested in contributing to research on Heart Health?
We are currently searching for volunteers to participate in a research study!
You may be eligible if you:
● Are 22 years of age or older
● Have no history of hypertension (high blood pressure)
Your role in the study:
Wear the study provided watch
Attend 3 virtual study visits
Complete daily home blood pressure monitoring for approximately 4 weeks
Return the study equipment
if interested click on the link below:
Sign Up for Message Alerts and Get Notified When New Clinical Trials Are Announced !
How do you Qualify for Strep Throat Study?
How do you Qualify for the Adolescent Wheezing Study?
The goal of clinical research is to develop knowledge that improves human health or increases understanding of human biology. People who take part in clinical research make it possible for this to occur. The path to finding out if a new drug is safe or effective is to test it on patients in clinical trials. The purpose of ethical guidelines is both to protect patients and healthy volunteers, and to preserve the integrity of the science.
Informed consent is the process of learning the key facts about a clinical trial before deciding whether to participate. The process of providing information to participants continues throughout the study. To help you decide whether to take part, members of the research team explain the study. The research team provides an informed consent document, which includes such details about the study as its purpose, duration, required procedures, and who to contact for various purposes. The informed consent document also explains risks and potential benefits.
If you decide to enroll in the trial, you will need to sign the informed consent document. You are free to withdraw from the study at any time.
Most, but not all, clinical trials in the United States are approved and monitored by an Institutional Review Board (IRB) to ensure that the risks are minimal when compared with potential benefits. An IRB is an independent committee that consists of physicians, statisticians, and members of the community who ensure that clinical trials are ethical and that the rights of participants are protected. You should ask the sponsor or research coordinator whether the research you are considering participating in was reviewed by an IRB.
Deciding to Participate in Clinical Trials
Innovation Clinical Trials
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