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To the participants:
Research, study, or trial are similar when it comes to clinical operation.
You must know that there are reasons to participate in clinical research. Without you, it is almost impossible.
New treatment and cure are tested during clinical study before they are available in the market.
Participants of the clinical research may not be assured of treatment, but there are numerous other benefits added during participation. 

Help uncover and advance medical innovation. Complete the create a profile form to get matched with new studies in your area. Our team will reach out soon to help determine your eligibility. You only need to complete the form once, regardless of how many studies you are interested in.
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​As a participant, you are closely watched by board-certified medical Doctor, you benefit from new condition about your health or any change. You would receive diagnostic and laboratory tests at no cost to you. Simultaneously, you help advance the medicine by enabling valuable data for the research trial. Moreover, participants are most of the time compensated for their travel time and time devoted to participation.
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Scroll Down for Studies That you can Participate Today


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Your travel expenses to the clinic including your time could be compensated; no health insurance needed, and your information are always kept confidential. Additionally, you get easy access to the research staffs even the MD for any question or concern. You can also withdraw the consent at any time of the study process.

​What is a clinical Research?
A clinical trial is a research study. It is designed to test if a medicine, vaccine, or medical device is effective and safe. A clinical trial may take place at a hospital, doctors’ office, or clinical research center. It is conducted by doctors, nurses, and other healthcare team members.
Most ideas for a new medicine or treatment start in a laboratory. This is called "preclinical" research. Scientists research a new product in the lab, sometimes over many years, before testing it in people. 
Only the most promising treatments go on to be studied, or investigated, in human beings. People volunteer to test these investigational treatments in clinical trials. These studies are designed to find answers to very specific health questions. 
How your participation helps?
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Thousands of people volunteer to participate in clinical trials every year. The reasons for participation vary, but all of them help to advance medicine. Some reasons include:
  • Medical supervision. Some people have a disease for which there is no approved treatment. They might join a clinical trial in the hopes of receiving an experimental medicine.
  • Contribute to future treatments. Many participants wish to help future patients. This has been reported by both patients and healthy volunteers.
  • Help improve the lives of others. Some people participate with the hope of helping others. The investigational drug or vaccine could benefit other patients and, in some cases, save lives.
What to expect in a clinical Research?
Clinical studies can take many years to develop and complete. Each one is designed differently. In general,
  1. Find out what kind of volunteers are being recruited to the study,
  2. Become informed about the specific details of the study, then determine whether you wish to give your consent to continue,
  3. Go through a screening process to find out if you are eligible to participate,
  4. If you are eligible, the study doctor and their staff will explain the study in detail and answer your questions. Their contact information will be included in your informed consent form.

You must understand before your consent:
Before you decide to participate in a clinical trial, you will go through a process called "informed consent". This is designed to help you learn the facts about the clinical trial before deciding whether to participate. 
You will be given detailed information about the study. This includes: 
  • the purpose, 
  • the possible risks, 
  • the potential benefits, 
  • how long it will take,
  • what procedures are required, and 
  • whom to contact with any questions or issues. 
Once you understand this information, you may decide to participate. At that point, you will be asked to give your consent. You will need to sign an “informed consent” document to confirm your decision. 
Then, you will go through a screening process to find out if you qualify to participate in the trial, based on the inclusion and exclusion criteria.

The Criteria:

Researchers plan studies under specific conditions considering many different factors like age, gender, the type and stage of the disease, any previous treatments a patient received, and whether they have other medical conditions. 
To find out if you might qualify for a study, ask about:
  • Inclusion criteria: Factors that determine whether you can be included, and
  • Exclusion criteria: Factors that could prevent you from participating.
US FDA on Clinical Trial
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STUDIES FOR PARTICIPANTS AND VOLUNTEERS Get Pay for Your Time
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Clinical Study on Clostridioides difficile infection (CDI) or C. Diff.

​The RESTORATiVE303 Study is a clinical research study that is exploring an investigational drug to restore the microbiome (the bacteria that live in your gut) in people with recurrent Clostridioides difficile infection (CDI). CDI is an infection of the large bowel (a part of your digestive system) caused by the bacteria Clostridioides difficile. Symptoms include diarrhea, stomach pain, nausea, vomiting, fever, and weight loss. 
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Teens Birth Control Study and The Effect on Bone Density

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Teenagers' Birth Control and Bone Density Clinical Research. Age 14 - 17
This study is active 

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