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Central and Peripheral Adiposity and Iron Absorption

F

Federal Institute of Technology (ETH) Zurich

Status

Completed

Conditions

Iron-deficiency
Adiposity

Treatments

Other: Stable iron isotopes

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

121 patients

Sex

Female

Ages

20 to 55 years old

Volunteers

Accepts Healthy Volunteers

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
  • smoking
  • blood donation or surgery within the last 4 months.

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

121 participants in 3 patient groups

normal-weight
Active Comparator group
Treatment:
Other: Stable iron isotopes
peripheral adiposity
Experimental group
Treatment:
Other: Stable iron isotopes
central adiposity
Experimental group
Treatment:
Other: Stable iron isotopes

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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