№ files_lp_4_process_3_125677
Clinical trial protocol section describing participant recruitment procedures, eligibility criteria, enrollment workflow, and retention strategies for a controlled study evaluating American Ginseng in adults with ulcerative colitis.
Study duration: 12 weeks
Location: South Carolina, United States
Clinical site: Prisma Health IBD Clinic
Participating institution: University of South Carolina
Medical specialty: Gastroenterology
Disease focus: Ulcerative colitis
Intervention: American Ginseng
Study design: Double-blind placebo-controlled clinical trial
Planned sample size: 80 participants
Lead clinical collaborator: Dr. Joseph Meserve
Participant population: Adults aged 18 years and older with confirmed ulcerative colitis on stable 5-ASA therapy
Primary recruitment source: Prisma Health Gastroenterology and Hepatology patient database
Recruitment coordination: USC research team and Prisma Health staff
Inclusion criteria: Confirmed ulcerative colitis diagnosis, UCDAI score greater than 3, stable 5-ASA therapy, informed consent
Exclusion criteria: Crohn’s disease or other IBD conditions, biologic or small molecule immunotherapy use, pregnancy or breastfeeding, active infection, active malignancy, investigational drug participation, ginseng allergy, medications causing interaction risks
Participant compensation: Up to $200 via Visa gift cards
Data collection: Blood, stool, and urine samples
Recruitment methods: Patient database identification, physician referrals, brochures and flyers, clinic outreach, online announcements
Retention measures: Participant education, regular communication, flexible scheduling, incentives, community engagement
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.

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