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  • About
    • Staff
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About Clinical Research
Study #49122

This study will be evaluating the nicotine levels and flavors in five (5) different oral nicotine pouch products in adult users.

Are You a Good Fit?

Men & Women, 22 - 65 years

Regular smokeless tobacco user for at least one year

Use at least 1/2 a can per day

BMI (Body Mass Index) must be between 18 - 40

Willing and able to use ALL study products for at least 45 minutes

  • Receive up to $3,500 for your participation in this study

What are the Time Requirements?

This study will consist of 5-day at home product trial run plus a 7-day inhouse stay. Study dates are as follows:
Group Groups 1 & 2
Visit Dates
Stay
Monday, March 6, 2023 - Sunday, March 12, 2023

How Much: $3,500 on Wednesday, March 15, 2023

Group Groups 3 & 4
Visit Dates
Stay
Wednesday, March 15, 2023 - Tuesday, March 21, 2023

How Much: $3,500 on Wednesday, March 22, 2023

Group Groups 5 & 6
Visit Dates
Stay
Thursday, March 23, 2023 - Wednesday, March 29, 2023

How Much: $3,500 on Wednesday, April 5, 2023

Group Group 7
Visit Dates
Stay
Tuesday, April 4, 2023 - Monday, April 10, 2023

How Much: $3,500 on Wednesday, April 12, 2023

Group Group 8
Visit Dates
Stay
Thursday, April 27, 2023 - Wednesday, May 3, 2023

How Much: $3,500

BMI Calculator

BMI Calculator Simple

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Referral Program

Do not forget our REFERRAL PROGRAM. Earn at least $200 for every new participant you refer who completes a study.*

*No referral bonuses are paid out for outpatient vaccine studies.
Middle Age Couple

All study dates are tentative and subject to change.

We will update the clinical research studies list weekly. Be sure to check with us either by calling or going online. Call (417) 831-2048 or visit 417studies.com for more information. You can also visit the Screening and Recruitment Center located at 2025 W. Sunshine Street, L-109. Office hours are Monday through Friday from 8 a.m. to 5 p.m.

• Female subjects who are heterosexually active and of childbearing potential must have been using one of the following forms of contraception and agree to continue using it through completion of the study:
– hormonal (e.g., oral, vaginal ring, transdermal patch, implant, injection) consistently for at least 3 months prior to Check-in,
– double barrier (e.g., condom with spermicide or diaphragm with spermicide) consistently for at least 2 weeks prior to Check-in,
– intrauterine device for at least 3 months prior to Check-in,
– exclusive partner who has been vasectomized for at least 6 months (inclusive) prior to Check-in.

• Female subjects of childbearing potential who are not currently engaging in heterosexual intercourse must agree to use one of the above methods of birth control through completion of study, in the event that they have heterosexual intercourse during the course of the study.

• Female subjects who are of nonchildbearing potential must have undergone one of the following sterilization procedures at least 6 months prior to Check-in:
– hysteroscopic sterilization with documentation of success with hysterosalpingogram;
– bilateral tubal ligation or bilateral salpingectomy;
– hysterectomy;
– bilateral oophorectomy;
– or be postmenopausal with amenorrhea for at least 1 year prior to Check-in and have FSH levels consistent with postmenopausal status.

If you have previously submitted an application, call 417-831-2048 to enroll. Or click on the button below to submit your application now.

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QPS Missouri

QPS Study Campus
1820 W. Mount Vernon Street
Springfield, MO 65802

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2025 W. Sunshine Street, L-109
Springfield, MO 65807

Hours of Operation:
Monday – Friday
8 a.m. – 5 p.m.

Call us at 417.831.2048

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