Actively Recruiting
Acceptability, Adherence, and Impact on the Bioavailability of Iron and Zinc of the Dietary Supplements Goodphyte IB Defense and Goodphyte Immunity in Adults With Chronic Diseases.
Led by University of Thessaly · Updated on 2026-02-02
100
Participants Needed
1
Research Sites
33 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary objective of the present postdoctoral research is to evaluate the acceptability and adherence of two dietary supplements containing microbial phytase, Goodphyte IB Defense and Goodphyte Immunity, in adult individuals with chronic diseases, namely Idiopathic Inflammatory Bowel Diseases (IIBD)-that is, Crohn's disease (CD) or Ulcerative Colitis (UC)-Arterial Hypertension (AH), Anemia (AN), or Multiple Sclerosis (MS). Secondarily, this study will investigate potential changes in iron and zinc absorption following phytase supplementation in these individuals and, consequently, possible changes in their quality of life.
CONDITIONS
Official Title
Acceptability, Adherence, and Impact on the Bioavailability of Iron and Zinc of the Dietary Supplements Goodphyte IB Defense and Goodphyte Immunity in Adults With Chronic Diseases.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with Crohn's disease in remission, stable treatment type for at least 3 months, stable dosage for the last month
- Adults with Ulcerative colitis in remission, stable treatment type for at least 3 months, stable dosage for the last month
- Adults with hypertension having systolic blood pressure 130-139 mmHg or diastolic blood pressure 80-89 mmHg, controlled by lifestyle changes without symptoms and no antihypertensive medication
- Adults with anemia meeting defined hemoglobin, serum iron, and ferritin levels, with manageable fatigue, weakness, or dizziness and no severe clinical consequences
- Adults with multiple sclerosis in remission, stable treatment type for at least 3 months, stable dosage for the last month
You will not qualify if you...
- Pregnancy or breastfeeding
- Current use of antibiotics or antibiotic use within the past month
- Current use of other probiotic, prebiotic, or synbiotic supplements
- Current use of iron and/or zinc supplements
- Change in pharmacological treatment type within the past three months
- Change in pharmacological treatment dosage within the past month
- Renal or hepatic disease
- Inability to provide informed consent or younger than 18 years old
- Insufficient understanding of the Greek language
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
School of Physical Education, Sport Science and Dietetics
Trikala, Thessaly, Greece, 42132
Actively Recruiting
Research Team
V
VAIOS SVOLOS, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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