2333 Town Ctr Dr,
Suite 250
Sugar Land, TX 77478
admin@rtxclinicalresearch.com
+1 346-375-4152
Patient Information
Participating in clinical trials offers numerous benefits, both for individual participants and the broader community:
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Access to Cutting-Edge Treatments: Participants often gain early access to new therapies and treatments that are not yet available to the public, potentially benefiting from the latest advancements in medical science.
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High-Quality Medical Care: Clinical trial participants receive close monitoring and care from a dedicated team of healthcare professionals, ensuring their health and safety throughout the study.
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Contribution to Medical Research: By participating in clinical trials, individuals contribute to the advancement of medical knowledge and the development of new treatments that can improve the lives of countless others.
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Personal Satisfaction: Many participants find personal satisfaction in knowing that they are playing a crucial role in advancing healthcare and potentially helping future generations.
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Diverse Representation: By joining a clinical trial, participants help ensure that research findings are applicable to a wide range of populations, leading to more effective and inclusive healthcare solutions.
Participating in clinical trials is a meaningful way to contribute to the future of medicine while potentially gaining access to innovative treatments and receiving top-notch medical care.
Joining a clinical trial at RTX Clinical Research is a straightforward process. Here’s a step-by-step guide to help you get started:
Explore Our Trials
Visit our website and navigate to the "Clinical Trials" section to see a list of ongoing and upcoming studies. Read the descriptions to find a trial that matches your interests and eligibility.
Step 1
Contact Us
If you find a trial you’re interested in, reach out to our team through the contact form on our website, email, or phone. Our staff will answer any questions you have and provide more information about the trial.
Step 2
Screening Process
Our team will conduct an initial screening to determine if you meet the basic eligibility criteria for the trial. This may include a phone interview or an online questionnaire.
Step 3
Informed Consent
If you are eligible, we will schedule an appointment for you to come in and learn more about the trial. During this visit, we will provide detailed information about the study, including its purpose, procedures, potential risks, and benefits. You will have the opportunity to ask questions and discuss any concerns. If you decide to participate, you will sign an informed consent form.
Step 4
Baseline Assessment
Before the trial begins, you will undergo a baseline assessment. This may involve physical exams, medical history review, and other tests to establish your health status before starting the trial.
Step 5
Participation
Once the baseline assessment is complete, you will begin participating in the trial according to the study protocol. This may involve regular visits to our site, taking medications, or undergoing specific procedures. Our team will closely monitor your health and progress throughout the study.
Step 6
Follow-Up
After the trial is completed, you may have follow-up visits to monitor your health and collect additional data. Our team will keep you informed about the results of the study and any potential long-term follow-up.
Step 7
By following these steps, you can join a clinical trial and contribute to important medical research while receiving excellent care from our experienced team. If you have any questions or need assistance, feel free to contact us!
