Skip to main content
Clinical Trials/NCT03642223
NCT03642223CompletedNot Applicable

Relation Btw Adiposity, Inflammation & Iron Absorption:Comparison Btw Central & Peripheral Adiposity

Swiss Federal Institute of Technology1 site in 1 country121 target enrollmentStarted: September 10, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
121
Locations
1
Primary Endpoint
Fractional and total iron absorption

Study Overview

Brief Summary

Adiposity is a state of sub-clinical inflammation, thus hepcidin is increased in adiposity, often leading to iron deficiency in this population group. Central adiposity is generally considered having a greater negative effect on health compared to peripheral adiposity. Whether this can be also seen in hepcidin and thereby in iron absorption is uncertain.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
20 Years to 55 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • either normal-weight (BMI 18-25kg/m2) or overweight/obese (BMI 28-50kg/m2) with either central or peripheral fat deposits based on DEXA

Exclusion Criteria

  • Iron Supplement or antibiotic intake within 2 weeks before study start
  • diagnosed chronic disease or gastrointestinal disorders
  • regular use of medication (except contraceptives)
  • pregnancy
  • lactation
  • blood donation or surgery within the last 4 months.

Arms & Interventions

central adiposity

Experimental

Intervention: Stable iron isotopes (Other)

peripheral adiposity

Experimental

Intervention: Stable iron isotopes (Other)

normal-weight

Active Comparator

Intervention: Stable iron isotopes (Other)

Outcomes

Primary Outcomes

Fractional and total iron absorption

Time Frame: 14days after the administration of the test meal

Secondary Outcomes

  • Serum IL-6(at baseline)
  • Serum AGP(at baseline)
  • Serum Hepcidin(at baseline)
  • Serum ferritin(at baseline)
  • Serum TfR(at baseline)
  • Serum CRP(at baseline)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Prof. Michael B. Zimmermann

Prof. Dr. med.

Swiss Federal Institute of Technology

Study Sites (1)

Loading locations...

Similar Trials