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  • Register with Our Database

    Registration form here.

    Get started on the volunteer process by registering your basic information with our database. This information is provided to help us determine your eligibility for current and future studies.

    If you have registered with Prism in the past, please call Dayna 651-724-5047 to update your profile or learn about available studies.

    Find the registration form here

     Unfortunately at this time, Prism can not allow volunteers who live over 200 miles away to participate in research studies. If you live out of state or over 200 miles away please call Geoff at 651-641-2911 with questions. 

    We will not share or sell this info with any third party.

    Thanks for your interest!

  • Upcoming Studies

     

     

     Prism has a variety of upcoming studies to participate in: 

    • Long inpatient stays for healthy males and females; Age 18-45 years old
    • Liver Impairment 
    • Kidney Impairment 

    To be put on the call list and receive more information, when available, please contact Dayna at daynas@prismresearchinc.com or Lindsay at lindsayd@prismresearchinc.com.

  • Diagnosed with Liver Impairment?

    Prism Research has upcoming studies for individuals diagnosed with liver impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of liver impairment when compared to volunteers with normal liver function.

     If you or someone you know has been diagnosed with liver impairment and are interested in being considered for these studies, please contact Dayna at 651-724-5047 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

    Please contact Dayna at 651-724-5047 or daynas@prismresearchinc.com

     

  • Diagnosed with Kidney Impairment?

    Prism Research has upcoming studies for individuals diagnosed with kidney impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of kidney impairment when compared to volunteers with normal kidney function.

     If you or someone you know has been diagnosed with kidney impairment and are interested in being considered for these studies, please contact Lindsay at 651-368-3360 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

    Please contact Lindsay at 651-368-3360 or lindsayd@prismresearchinc.com

  • Refer Your Friends & Family to Participate

    Simply help us get the word out about Prism Clinical Research and we’ll give you $100 for every friend you refer that completes a study.

    It’s that easy! Make money with each referral, and there’s no limit to how many friends you can refer!

    Rules:

    • Subject must qualify for a study.
    • Subject may not be referred more than one time.
    • Subjects eligible for Referral: (1) Must not be in Prism Clinical Research database; (2) Must not have participated in any prior study at Prism.
    • In the event that a subject is referred by multiple people, the first person who referred will receive payment.
    • Eligibility will be determined by Prism. Prism reserves the right to revise or eliminate this program at any time without notice.

     

     

  • Multiple Sclerosis: Clinical Research Study

    Multiple Sclerosis Study

     

    PRISM CLINICAL RESEARCH 

    Purpose: 

    • To evaluate the safety and tolerability of an investigational drug in individuals with Progressive Forms and/or Relapsing Forms of Multiple Sclerosis.

     

    GENERAL STUDY REQUIREMENTS:   

    • Men and Women, between the ages of 18 and 55.
    • Clinical diagnosis of Primary or Secondary multiple sclerosis or Relapse Remitting or Secondary-Progressive multiple sclerosis.

     

    STUDY DURATION: 

    • 17 Clinic Visits over the course of 76 weeks

     

    METHOD OF ADMINISTRATION:

    • Intravenous Administration

     

    Compensation for Study Participation Time  and Travel

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1812

    Renal Impairment Study

    Clinical RESEARCH study: 1812

     

    PRISM Clinical RESEARCH

     

     

     

     

    Purpose:

    •  A research study to evaluate the safety and tolerability of an investigational drug in individuals with renal impairment compared with individuals without renal impairment.

     

    GENERAL STUDY REQUIREMENTS:

    •  Men and Women Who are not able to become pregnant, between the ages of 18 to 75 with a BMI between 17.5 and 36 kg/m2.
    •  Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION:

    •  In Clinic Stay: 6 nights/7 days.
    •  Clinic Visits: up to 3 including screening and possible Follow-up visit.
    •  Total study duration is approximately 6 weeks (including a 14-day screening period).

     

    METHOD OF ADMINISTRATION:

    •  Oral Administration

     

    STUDY COMPENSATION:

    •  Compensation for Study Participation Time Up To: $2,385.00

     

    RECRUITMENT CONTACT:

     

     To prequalify, click here

  • Liver Impairment: Clinical Research Study 1817

    LIVER IMPAIRMENT STUDY

    CLINICAL RESEARCH STUDY: 1817

    PRISM CLINICAL RESEARCH

    PURPOSE:

    • To determine how the investigational drug is absorbed, broken down, and removed from the body in volunteers with abnormal liver function compared to volunteers with normal liver function.

     

    GENERAL STUDY REQUIREMENTS:

    • Men and women between the ages of 18 and 80 years old.
    • Liver Impairment volunteers: must have mild/moderate/severe liver impairment due to diagnosed liver disease.
    • Healthy volunteers: must be healthy; not being evaluated or treated for any medical conditions.

     

    STUDY DURATION:

    • 1 In-Clinic Stay: Lasting 8 nights/ 9 days
    • Clinic Visits: 1(screening)
    • Total Study Duration is Approximately 39 days, including screening

     

    METHOD OF ADMINISTRATION:

    • Oral Administration

     

    STUDY COMPENSATION:

    • Compensation for Study Participation may be provided for time and travel up to $2620.00

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1822

     

    Renal Impairment Study

    Clinical RESEARCH study: 1822

     

    PRISM CLINICAL RESEARCH

     

     

     Purpose:

    •  To assess the pharmacokinetics and to evaluate the safety of an investigational drug in individuals with severe renal impairment versus individuals with normal renal function.

     

    GENERAL STUDY REQUIREMENTS:

    •  Men and Women, between the ages of 18 and 80
    •  Medical conditions and medications must be stable in the opinion of the study doctor.
    •  Volunteers must agree to use contraception, if applicable

     

    STUDY DURATION:

    • In Clinic Stay: 1 in clinic stay of approximately 72 hours, including 24 hours infusion of study drug.
    •  Clinic Visits: 3, including screening visit, visit for PK sample collections and follow up visit.
    •  Total study duration is approximately 38 days (including a 21-day screening period).

     

    METHOD OF ADMINISTRATION:

    •  Intravenous

     

    REIMBURSEMENT:

    •  Reimbursement  for reasonable expenses in connection with your Study Participation Up To $1240.

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1902

    Renal Impairment Study

    Clinical RESEARCH study: 1902

     

    PRISM RESEARCH

     

     

    Purpose: 

    •  To evaluate the safety and tolerability of an investigational drug being developed to ease symptoms of pain and heavy menstrual bleeding associated with endometriosis and uterine fibroids in individuals who have been diagnosed with different levels of kidney impairment compared with individuals with normal kidney function

     

    GENERAL STUDY REQUIREMENTS:   

    •  Women who are 18 years or older with a BMI between 18 to 42
    •  Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION: 

    •  In Clinic Stay: 6 night/ 7 days (groups 1-4)
    •  In Clinic Stay: 4 night/5 days (group 5)
    •  Return Clinic Visits: 2 including screening
    •  Total study duration is approximately 42 days

     

    METHOD OF ADMINISTRATION:

    •  A single oral dose

     

    STUDY COMPENSATION: 

    •  Compensation for Study Participation Time and Travel Up To: $2170.00 (groups 1-4) and $1570.00 (group 5)

     

    RECRUITMENT CONTACT:

     

  • Seasonal Allergies: Clinical Research Study 1908

    Seasonal Allergy Study

    Clinical RESEARCH study: 1908

     

    PRISM RESEARCH

     

     

     

    Purpose: 

    •  To evaluate the safety and tolerability of an investigational drug in individuals with seasonal allergies.

     

    GENERAL STUDY REQUIREMENTS:   

    •  Men and Women, between the ages of 18-45
    •  Must be healthy and not taking any medications.
    •  Volunteers must agree to use contraception, if applicable
    •  Must have a BMI of 18.5-35kg/m²

     

    STUDY DURATION: 

    •  In Clinic Stay: 3 in clinic stays of 2 nights/ 3 days each.
    •  Return Clinic Visits: 1 screening visit.
    •  Total study duration is approximately 45 (including a 28-day screening period).

     

    METHOD OF ADMINISTRATION:

    •  Intramuscular and nasal spray

     

    STUDY COMPENSATION: 

    •  Compensation for Study Participation Time Up To: $1500.00

     

    RECRUITMENT CONTACT:

     

     

     

  • Healthy Clinical Research Study 1909

    HEALTHY CLINICAL RESEARCH STUDY 1909

    MALES AND FEMALES

     

    PURPOSE:

    •  To evaluate Vitamin D levels in healthy adults

     

    GENERAL REQUIREMENTS:

    • Men and women; 22 years old or older
    • BMI between 18-29.9
    • Medication will be approved on a case by case basis

     

    STUDY DURATION

    • 1 outpatient visit lasting approximately 3 hours

     

    METHOD OF ADMINISTRATION:

    • This is a sample collection study; no study drug will be administered.

     

    STUDY COMPENSATION:

    • Compensation for Study Participation Time Up To: $75.00

     

    RECRUITMENT CONTACT: Dayna 651-724-5047 or daynas@prismresearchinc.com

     

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    Use the link below:↓

    https://www.facebook.com/PrismResearch/

Your Partner in Research

Prism Clinical Research is a phase I-IV clinical research facility located in the heart of the Twin Cities metro area, in a community of over 3 million residents with a rich tradition in medical care advancements.


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Prism is situated in a diverse and vibrant metro area with a population base of over 3.5 million.

Icon 24 We’ve worked hard to grow a diverse database of specialty demographic populations, so we’re equipped to conduct virtually any type of study.

 

We take pride in our highly trained, dedicated staff, our state-of-the-art facility, and a volunteer database that ensures your trial expectations are met or exceeded. From site assessment to trial closeout, our commitment to your success starts from the first conversation. Prism Clinical Research believes that clear, honest communication is critical to ensuring trial success. So, though we are grateful for consideration for your trial needs, we want to be certain Prism Clinical Research is the right fit for your project. Our team will quickly evaluate your trial needs and determine enrollment, timelines and resources. Honest protocol review & site assessment will be the first priority.

Start the conversation. Get in touch with Prism Clinical Research.


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Our Mission

Prism Clinical Research wants to be our client’s first choice for research services. We accomplish this by considering our client a partner for their trial objectives. Prism Clinical Research is committed to providing timely and accurate trials. It is our staff’s passion for making a difference that allows us to meet and exceed our client’s expectations.

Please provide us with your contact information (below) and will get back to you as soon as possible.

If you have a general question, check Volunteer FAQ for an answer. If you're unsure of who to contact, please visit the Contact Us page.

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