Learn About Clinical Trials
Explore how medical studies work, why they’re important, and what Pillar Clinical Research can do for you.
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Overview
What is Clinical Research?
Clinical research is a branch of healthcare science that involves investigating new treatments, therapies, and interventions to improve patient care. It helps researchers better understand diseases and develop innovations in medicine.
Why Are Clinical Trials Important?
Clinical trials are essential for testing the safety and effectiveness of new medical treatments and devices. They are a critical step in advancing medical knowledge and ensuring that new therapies can benefit patients.
Why Should I Participate?
Pillar Clinical Research provides expert conduct of early- and late-phase trials for both inpatient and outpatient clinical studies. Founded in 2008, Pillar is distinguished for exceptional participant care, superior research services, and dedication to advancing pharmaceutical development. Pillar is proud of a long history collaborating with industry sponsors, Contract Research Organizations (CROs), industry vendors, and clinical-based technology providers.
Medical studies elevate public health by advancing the latest pharmaceutical treatments and therapies. Your involvement is crucial to this process, contributing to scientific knowledge and leading to healthcare innovation.
What are the different phases of medical studies?
- Phase 1: These clinical trials test a new treatment on a small group of participants to evaluate safety, dosage, and side effects.
- Phase 2: This stage of medical research focuses on the effectiveness of the treatment in a larger group while continuing to assess safety.
- Phase 3: These clinical studies compare the new treatment to existing treatments, involving an even larger group to confirm effectiveness, monitor side effects, and gather data for regulatory approval.
- Phase 4: Conducted after a treatment is approved, these trials gather long-term safety and effectiveness data in broader populations.
Who manages clinical trials?
- Investigators: These individuals lead and oversee the clinical trial, ensuring it’s conducted ethically, that participants’ safety is prioritized, and that accurate data is collected.
- Sponsors: Typically, these are organizations (like pharmaceutical companies or research institutions) that fund the trial and are responsible for initiating and managing the study.
- IRBs (Institutional Review Boards): Under federal regulation from the FDA and the HHS Office for Human Research Protections, independent committees called IRBs review and approve clinical trials to ensure they are ethical and that participants’ rights and safety are protected.
How safe is medical research?
Clinical trials follow strict safety protocols, including rigorous ethical review by IRBs, informed consent processes, close monitoring of participants’ health, and regular reporting of any adverse effects. Trials are also governed by federal regulations and guidelines to protect participants.
Participants have the right to be fully informed about the trial, including its risks and benefits, and to give or withdraw consent at any time. These volunteers are also entitled to privacy and confidentiality regarding their personal health information, and they can leave the study without any penalty or impact on their regular medical care.
Overview
What is Clinical Research?
Clinical research is a branch of healthcare science that involves investigating new treatments, therapies, and interventions to improve patient care. It helps researchers better understand diseases and develop innovations in medicine.
Why Are Clinical Trials Important?
Clinical trials are essential for testing the safety and effectiveness of new medical treatments and devices. They are a critical step in advancing medical knowledge and ensuring that new therapies can benefit patients.
Why Should I Participate?
Pillar Clinical Research provides expert conduct of early- and late-phase trials for both inpatient and outpatient clinical studies. Founded in 2008, Pillar is distinguished for exceptional participant care, superior research services, and dedication to advancing pharmaceutical development. Pillar is proud of a long history collaborating with industry sponsors, Contract Research Organizations (CROs), industry vendors, and clinical-based technology providers.
Medical studies elevate public health by advancing the latest pharmaceutical treatments and therapies. Your involvement is crucial to this process, contributing to scientific knowledge and leading to healthcare innovation.
What are the different phases of medical studies?
- Phase 1: These clinical trials test a new treatment on a small group of participants to evaluate safety, dosage, and side effects.
- Phase 2: This stage of medical research focuses on the effectiveness of the treatment in a larger group while continuing to assess safety.
- Phase 3: These clinical studies compare the new treatment to existing treatments, involving an even larger group to confirm effectiveness, monitor side effects, and gather data for regulatory approval.
- Phase 4: Conducted after a treatment is approved, these trials gather long-term safety and effectiveness data in broader populations.
Who manages clinical trials?
- Investigators: These individuals lead and oversee the clinical trial, ensuring it’s conducted ethically, that participants’ safety is prioritized, and that accurate data is collected.
- Sponsors: Typically, these are organizations (like pharmaceutical companies or research institutions) that fund the trial and are responsible for initiating and managing the study.
- IRBs (Institutional Review Boards): Under federal regulation from the FDA and the HHS Office for Human Research Protections, independent committees called IRBs review and approve clinical trials to ensure they are ethical and that participants’ rights and safety are protected.
How safe is medical research?
Clinical trials follow strict safety protocols, including rigorous ethical review by IRBs, informed consent processes, close monitoring of participants’ health, and regular reporting of any adverse effects. Trials are also governed by federal regulations and guidelines to protect participants.
Participants have the right to be fully informed about the trial, including its risks and benefits, and to give or withdraw consent at any time. These volunteers are also entitled to privacy and confidentiality regarding their personal health information, and they can leave the study without any penalty or impact on their regular medical care.
Overview
What is Clinical Research?
Clinical research is a branch of healthcare science that involves investigating new treatments, therapies, and interventions to improve patient care. It helps researchers better understand diseases and develop innovations in medicine.
Why Are Clinical Trials Important?
Clinical trials are essential for testing the safety and effectiveness of new medical treatments and devices. They are a critical step in advancing medical knowledge and ensuring that new therapies can benefit patients.
Why Should I Participate?
Pillar Clinical Research provides expert conduct of early- and late-phase trials for both inpatient and outpatient clinical studies. Founded in 2008, Pillar is distinguished for exceptional participant care, superior research services, and dedication to advancing pharmaceutical development. Pillar is proud of a long history collaborating with industry sponsors, Contract Research Organizations (CROs), industry vendors, and clinical-based technology providers.
Medical studies elevate public health by advancing the latest pharmaceutical treatments and therapies. Your involvement is crucial to this process, contributing to scientific knowledge and leading to healthcare innovation.
What are the different phases of medical studies?
- Phase 1: These clinical trials test a new treatment on a small group of participants to evaluate safety, dosage, and side effects.
- Phase 2: This stage of medical research focuses on the effectiveness of the treatment in a larger group while continuing to assess safety.
- Phase 3: These clinical studies compare the new treatment to existing treatments, involving an even larger group to confirm effectiveness, monitor side effects, and gather data for regulatory approval.
- Phase 4: Conducted after a treatment is approved, these trials gather long-term safety and effectiveness data in broader populations.
Who manages clinical trials?
- Investigators: These individuals lead and oversee the clinical trial, ensuring it’s conducted ethically, that participants’ safety is prioritized, and that accurate data is collected.
- Sponsors: Typically, these are organizations (like pharmaceutical companies or research institutions) that fund the trial and are responsible for initiating and managing the study.
- IRBs (Institutional Review Boards): Under federal regulation from the FDA and the HHS Office for Human Research Protections, independent committees called IRBs review and approve clinical trials to ensure they are ethical and that participants’ rights and safety are protected.
How safe is medical research?
Clinical trials follow strict safety protocols, including rigorous ethical review by IRBs, informed consent processes, close monitoring of participants’ health, and regular reporting of any adverse effects. Trials are also governed by federal regulations and guidelines to protect participants.
Participants have the right to be fully informed about the trial, including its risks and benefits, and to give or withdraw consent at any time. These volunteers are also entitled to privacy and confidentiality regarding their personal health information, and they can leave the study without any penalty or impact on their regular medical care.
Meet our team of expert clinicians, clinical researchers, and administrators. Our experience and warmth create an environment of comfort and professionalism.
Frequently Asked Questions
Am I eligible to participate in a clinical trial?
Each clinical trial has specific inclusion and exclusion criteria that define who can participate. Factors such as age, gender, medical history, current health condition, current medications, and previous treatments typically determine eligibility. We will conduct a screening process to ensure you meet the requirements and understand your role and rights.
What are the risks and benefits of participating in a clinical trial?
Clinical trials offer benefits like access to new treatments before they’re widely available, close monitoring by healthcare professionals, and contributing to medical research. However, there are risks, including unknown side effects, possible ineffectiveness of the treatment, or the time and commitment required. Researchers will explain all potential risks and benefits during the informed consent process.
Will I be compensated for participating in a clinical trial?
Compensation varies by trial. Some clinical trials provide participants with a stipend or reimburse expenses such as travel, time off work, or childcare. However, not all trials offer compensation. Compensation details will be outlined before you agree to participate.
How many check-up visits are usually included in a clinical trial?
The number of check-up visits can vary depending on the study. Some trials may require weekly or monthly visits, while others may have fewer, spaced-out appointments. The trial coordinator will provide a detailed schedule before you enroll.
What if I don’t have transportation?
Transportation to and from your home for both pre-screening visits and visits during a clinical research trial can be provided by Pillar Clinical Research. Don’t let transportation concerns stop you from reaching out to us.
How long does a clinical trial usually last?
The duration of a clinical trial varies depending on its phase and the type of treatment being studied. Some trials last a few weeks or months, while others may span multiple years to assess long-term effects and safety.
Will I continue to see my regular doctor or therapist?
Yes, participants can usually continue to see their regular doctor or therapist during the trial. The clinical trial team will coordinate with your healthcare providers to ensure comprehensive care throughout your participation.
Can I leave a clinical trial once it has started?
Yes, participation in a clinical trial is voluntary, and you can withdraw at any time without penalty. If you choose to leave, it is important to notify the research team so they can take steps to ensure your safety and, if necessary, adjust your treatment accordingly.
What happens after the clinical trial ends?
After the trial ends, the research team will provide follow-up care and share key findings. While there may be some cases where participants may continue to receive the treatment, this is a rare exception, and participants should not count on the investigational medicine or therapy to be continued.
This is your chance to make a difference.
Dallas Clinical Research Center
(214) 396-4844
630 N Coit Rd, #2200 | Richardson, TX 75080
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Chicago Clinical Research Center
(224) 534-7332
3400 N Pulaski Rd | Chicago, IL 60641
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NW Arkansas Clinical Research Center
(479) 367-2688
3200 NE Redhawk Dr | Bentonville, AR 72712
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Central Arkansas Clinical Research Center
(501) 307-1919
19 Remington Dr | Little Rock, AR 72204
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Mon-Fri: 8:30am-5pm
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Carol Witham
CEO, Pillar Clinical Research
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