Actively Recruiting
The Effect of Chitin and Ascorbic Acid on Dietary Iron Absorption From Tenebrio Molitor Larvae in Young Women
Led by Swiss Distance University of Applied Sciences · Updated on 2025-05-31
25
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
Sponsors
S
Swiss Distance University of Applied Sciences
Lead Sponsor
S
Swiss Federal Institute of Technology
Collaborating Sponsor
AI-Summary
What this Trial Is About
Iron plays a crucial role in many body functions, including oxygen transport, DNA repair, and muscle metabolism. Iron deficiency, especially among women of childbearing age, adolescents, and young children, is a widespread concern caused by factors like low dietary intake and poor absorption. This trial investigates how chitin, a natural component found in insects, affects iron absorption from insect-based foods and how adding ascorbic acid influences this process. The study uses stable iron isotopes to measure iron absorption specifically from Tenebrio molitor larvae. Participants will consume vegetable soups prepared with different meals containing labeled T. molitor larvae or iron sulfate, with variations including added chitin and ascorbic acid. Seven meal types are tested, each differing in chitin content or ascorbic acid presence to evaluate their impact on iron absorption. The study follows a randomized design with single masking, comparing these meals to understand how chitin and ascorbic acid affect iron uptake. During the study, iron absorption is measured at multiple points: screening, day 16, day 32, and day 47. Researchers will also monitor blood markers such as hemoglobin, serum ferritin, transferrin receptor levels, and inflammation indicators through blood samples taken at the same intervals. The total participation duration is approximately 47 days, during which participants will undergo dietary interventions and regular laboratory assessments to evaluate iron status and absorption.
CONDITIONS
Brief Title
Effect of Chitin and Ascorbic Acid on Dietary Insect Iron Absorption
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female aged between 18-45 years
- Normal BMI (18.5 - 24.9 kg/m2)
- Body weight < 70 kg
- Low iron status (being in the lower half of the serum ferritin distribution at screening)
You will not qualify if you...
- Anaemia (hemoglobin < 12 g/dL)
- Inflammation (CRP > 5.0 mg/L)
- Pregnancy or intention to become pregnant during the study or within 30 days after the study
- Lactating up to 6 weeks before study start
- Chronic digestive, kidney, or metabolic diseases
- Antibiotics use in the last 4 weeks or during the study
- Mineral and vitamin supplements in the last 2 weeks or during the study
- Chronic medication use except oral contraceptives
- Blood transfusion, donation, or significant blood loss in last 4 months
- Participation in a stable isotope or any clinical study within last 30 days
- Food allergies, especially to crustacea, dust mites, seafood, gluten, milk, or eggs
- Smoking more than 1 cigarette per day
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 47 days
Participants consume different vegetable soup meals prepared with various forms of iron and chitin or ascorbic acid to study dietary iron absorption.
4 visits (in-person) on Days 0, 16, 32, and 47
Trial Site Locations
Total: 1 location
1
ETH Zürich
Zurich, Canton of Zurich, Switzerland, 8005
Actively Recruiting
Research Team
D
Diego Moretti, Prof.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
7
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