3093 - MASH (SW) Clinical Trials

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Campaign ID: 6251
Category: Research Trial
Payout: $32.00

Description:
Live Geos: https://partners.subjectwell.com/publishers/geos_report/382efff3-9ba5-40c4-aa06-af414bce9e55 Age Range: 18-75 Gender: Any Study Description: This study will test an investigational oral medication for Metabolic dysfunction-associated Steatohepatitis (MASH), formerly known as Non-Alcoholic Steatohepatitis (NASH). Participants will receive either the investigational oral medication or a placebo to be taken twice weekly for up to 11 months. Study procedures will include vital signs, physical examinations, blood draws, MRIs, liver biopsies, FibroScan, and electrocardiograms. Total participation will last up to 1 year and 2 months, with up to 14 doctor’s visits throughout the study. Eligibility for the study will be determined by the study doctor, following an in-person screening visits to the clinic. Trial-related procedures and study medication will be provided at no cost. QUESTIONS/ANSWERS - DO NOT GIVE TO TRAFFIC: 1. Have you been diagnosed with Metabolic Dysfunction-Associated Steatohepatitis (MASH), formerly referred to as Non-Alcoholic Steatohepatitis (NASH) or Fatty Liver Disease? - YES 2. Have you been diagnosed with Type I or Type II diabetes? - TYPE 2, NO, OR UNSURE 3. Do you have at least 2 of the following increased risk factors for MASH/NASH -High Blood Sugar -High Blood Pressure (≥130/85) -High Triglycerides (≥150mg/dL) -Currently being treated with medication for high triglycerides -Low levels of HDL cholesterol (the good cholesterol) -Obesity/overweight defined as the following: -Men: BMI ≥ 25 or waist circumference ≥ 40 inches -Women: BMI ≥ 25 or waist circumference ≥ 35 inches - YES 4. Are you willing and able to undergo liver biopsies and MRIs as part of the requirements to participate in the study? - YES

2858 - Severe Chronic Pruritus (Itchy Skin) (SW) Clinical Trials

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Campaign ID: 6250
Category: Research Trial
Payout: $60.00

Description:
Description Live Geos: https://partners.subjectwell.com/publishers/geos_report/8a730166-9e0b-4f39-8b79-5ccd36c6094c

2665 - Chronic Kidney Disease and High Blood Pressure Clinical Trial (SW)

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Campaign ID: 6248
Category: Research Trial
Payout: $52.00

Description:
Description Live Geos: https://partners.subjectwell.com/publishers/geos_report/2710209c-64c3-41be-b7c0-1add158aff11 Gender: All Ages: 18+ Study Description: This study is testing an investigational combination of two oral study medications in adults with chronic kidney disease (CKD) and high blood pressure. Participants will receive either an FDA-approved medication plus an investigational medication or placebo for 2 years. During the 2-year study treatment period, participants will complete 10 study visits. After the study treatment period, participants will have 2 visits after a 6-week follow-up period. Eligibility for the study will be determined by the study doctor following one or more in-person screening visits to the clinic. Study-related procedures and study medication will be provided at no cost. Qualifications: - Cannot have had dialysis in the last 3 months - Must be taking medication to lower your blood pressure, but blood pressure must still be high - Cannot have had a stroke, mini stroke (TIA), heart attack or been hospitalized for heart failure in the last 3 months - Cannot be currently pregnant or planning to become pregnant in the next 2 years - Cannot have type 1 diabetes

2903 - Major Depressive Disorder (SW) Clinical Trials

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Campaign ID: 6247
Category: Research Trial
Payout: $24.00

Description:
Study Description: This study is testing an investigational oral medication for major depression. Participants will receive a daily dose of either the study medication or its matching placebo for 4 weeks. Additional procedures include physical examination, vital signs and laboratory testing. Total participation will last approximately 10 weeks and would include 8 office visits throughout the study. Eligibility for the study will be determined by the study doctor following one or more in-person screening visits to the clinic. Trial-related procedures and study medication will be provided at no cost. Qualifications: - Depressive episode cannot have lasted >2 years - Cannot have a history of: heart attack, heart failure, or stroke

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