FAQ's

Your voluntary participation in a clinical trial provides invaluable medical information for yourself and others. Without volunteers, medical advances would not be possible and the safety and benefits of medications would not be ensured. If you wish to participate in a trial, specially qualified physicians and research staff will see you for an evaluation of your condition and determine if any current or future clinical trials may be right for you. All of this is provided for you at no cost.

The initial evaluation appointment allow time for you to meet with our medical staff to review and conduct a thorough medical evaluation which may include: Medical History Review, Vital Signs, Urine/Blood Test, along with other assessments that are standard to our intake process.  Please call at 425-453-0404 or email study.coordinator@nwcrc.net for more details.

Yes, transportation support is available if you live within 40 miles of our center. Please call at 425-453-0404 or email study.coordinator@nwcrc.net for more details.

Yes, compensation is reviewed during the initial evaluation visit. Please call at 425-453-0404 or email study.coordinator@nwcrc.net for more details.

Clinical trials are conducted with utmost safety measures to protect participants. Before a trial begins, it goes through a rigorous review process by ethics committees and regulatory authorities. Additionally, participants are closely monitored throughout the trial to ensure their well-being.

Some people participate in clinical trials because none of the standard (approved) treatment options have worked, or they are unable to tolerate certain side effects. Clinical trials provide another option when standard therapy has failed. Others participate in trials because they want to contribute to the advancement of medical knowledge.

Some clinical trials have a placebo group to compare the effects of an investigational medication to a control group.

Participation in a clinical trial is always voluntary. You have the right to leave the trial at any time without consequences or loss of regular medical care.

The duration of clinical trials is dependent and vary per study. Trials can range anywhere from a few weeks to a few years. This will be discussed thoroughly during the evaluation or call our office for further information.

As with any medical intervention, there may be risks associated with participating in a clinical trial. These risks will be thoroughly explained to you during the informed consent process, allowing you to make an informed decision.

Clinical trial eligibility criteria vary based on the study’s objectives and the medication or intervention being tested. Some trials may include participants with specific medical conditions, while others may require participants to be in good health. The study coordinator can help determine if you qualify for a particular trial.

Patient confidentiality is of utmost importance in clinical trials. All personal information and medical records are protected and kept confidential according to strict privacy regulations.

Stay up-to-date with the latest clinical trials by following us on Facebook and Instagram, where we share current news and information.

In general, participating in multiple clinical trials at the same time is not advisable. The study coordinator can guide you on appropriate participation based on your specific situation.