Wisdom Teeth Removal Study

Wisdom Teeth Removal Study

Do you need your wisdom teeth removed? CenExel CIT will soon be conducting a clinical research study of an investigational pain drug given after a no cost wisdom teeth removal.

What to expect:

Patients that qualify for the study may receive no cost wisdom teeth removal surgery by one of our board-certified Oral Surgeons, in our state-of-the-art facility. Qualified participants also receive study related care, and compensation for time and travel.

  • If our oral surgeons recommend you as a suitable candidate for this wisdom teeth study, we’ll discuss any surgical risks with you and if you are happy to participate schedule your surgery.
  • You may withdraw from the study at any time.
  • Wisdom teeth removal is an outpatient surgery that is performed under local anesthesia with laughing gas (nitrous oxide/oxygen analgesia).
  • Once the wisdom teeth are removed, the gums will be sutured, and gauze will be placed in the mouth.
  • Recovery instructions will be discussed with you after the surgery.



What are Wisdom Teeth?

The average adult has 32 teeth. The average mouth, however, holds only 28 teeth comfortably. The extra four molars at the back of your mouth are referred to as “wisdom teeth.”

Why Should You Consider Having Your Wisdom Teeth Removed?

Wisdom teeth removal is often needed because it’s common for wisdom teeth to not align properly when they begin to push through the surface of the gums. Wisdom teeth can grow in sideways, emerge only partially from the gum, or remain trapped between the gum area and bone.

Impacted wisdom teeth can reposition several times as they try to find a path that will allow them to fully emerge, all of which can cause swelling, stiffness, pain, and illness. Perhaps the biggest problem caused by wisdom teeth is the tumors or cysts that can form when the teeth remain impacted. These tumors or cysts destroy the nearby jawbone and healthy teeth.
Partially emerged wisdom teeth are also troubling, as they enable bacteria to grow in the opening around the teeth. This eventually can lead to infection in the mouth. Wisdom teeth that do emerge can cause other teeth to move, disrupting your orthodontic care or the natural alignment of your teeth.

Early removal of wisdom teeth is recommended so you can prevent these problems and lower the surgical risk that is associated with wisdom teeth removal

To be considered for the study, please fill out the form or call 951-801-7266.


No cost studies will soon be available for qualified participants.


No health insurance required


Compensation for time and travel TBD



Male / Female



State-of-the-Art Facilities

CIT is California’s premier clinical research organization. For over two decades, we’ve helped improve the quality of life for everyone by researching new medications and treatments. Our state-of-the-art facility is held to the highest standards of cleanliness and quality.

Board-Certified Physicians

Your safety is our greatest concern. Every procedure at CIT is overseen by expert medical staff and performed by some of the most well-respected board-certified physicians in the industry, each with many years of experience in their respective specialties.

Standard Procedures

Rest assured, you are not signing up for an “experimental” method. Cenexel CIT only performs standard surgery procedures as if you were at any other hospital or clinic. Our research is focused on the investigational medications given after that procedure.

Frequently asked questions

What is a CenExel Center of Excellence?

CenExel Centers of Excellence provide unparalleled medical and scientific support in the design and execution of clinical trials. Their attention to detail assures quality, reliable results and has helped CenExel to consistently achieve and exceed patient recruitment goals. They have conducted thousands of studies, the variety and complexity of which have resulted in a great depth of experience and insight for the principal investigators and research staff in each facility. CenExel Centers of Excellence deliver the engagement, expertise, and results to ensure that clients achieve their clinical research goals.

How do clinical trials work?

The study procedures and process will vary depending on the type of clinical trial you participate in. Before you begin a study, the process and all procedures for that study will be explained to you. Throughout the study, the Study Coordinator and the Principal Investigator will assist you and can answer any questions you have. They will check your health at the beginning of the trial, give you specific instructions for participating in the trial, monitor you carefully during the trial, and stay in touch with you after the study.

Some clinical trials involve more tests and doctor visits than you would normally have for your illness or condition. Your participation will be most successful if you carefully follow all instructions you are given and stay in contact with the research staff.

How safe are clinical studies?

There are many safeguards in place that all companies must follow when conducting clinical trials.

The Food and Drug Administration (FDA) is the regulatory agency that oversees all clinical research conducted in the United States. It is their responsible to protect the rights and as much as possible, the welfare of subjects participating in clinical trials. They ensure that data collected from clinical trials is of the highest quality and they are the agency that determines whether a new treatment should be sold in the US. Several organizations and individuals are governed by FDA regulations including clinical investigators, sponsors (the companies developing the treatments), Contract Research Organizations (companies that help conduct the studies), and Institutional Review Boards (groups that are responsible for ensuring the safety and welfare of study participants).

Good Clinical Practice (GCP) guidelines are another safeguard implemented to protect the safety of subjects. These guidelines encompass federal regulations and industry-accepted standards that govern clinical trials on humans. These regulations and standards apply to the conduct of the studies, record keeping, informed consent of subjects, collection of scientific data, and submission of information needed for the FDA to determine whether a new treatment should or should not be sold in the US. All companies must follow these guidelines when conducting clinical research.

An Institutional Review Board (IRB) is a committee that is formally tasked by an institution to review, approve, and monitor research involving human subjects. IRBs ensure that the risks to subjects are minimized; that subjects are adequately informed about the trial and the implications it will have on their treatment; that study protocols are modified, when necessary, to ensure safety; that risks are reasonable in relation to the anticipated benefits and the importance of the knowledge to be gained; that subject selection is equitable and that no classes of patients are discriminated against; that informed consent is obtained; that there is a provision for safety monitoring in the research plan; and that here are adequate provisions for the privacy and confidentiality for subjects and the data collected.

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