Clinical Trials Directory

Trials / Completed

CompletedNCT01985204

Iodine Supplementation in Obesity

Assessment of the Improvement of the Cardiovascular Risk Profile in Obese Women After Correction of Iodine Deficiency

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
162 (actual)
Sponsor
Swiss Federal Institute of Technology · Academic / Other
Sex
Female
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

The study hypothesis is that iodine supplementation will lower serum TSH and leptin concentrations and thereby improve the lipid and glucose profile.

Detailed description

The study will be a double blind, placebo controlled intervention study in obese women living in the Atlas foot mountains in Morocco, an iodine deficient area. Eligible subjects will be randomized into intervention and control group and will receive the respective supplement for 6 months. At baseline, midpoint and endpoint anthropometric as well as metabolic profile will be assessed. A health questionnaire will further be administered monthly when the tablets for the following month are distributed. Urine samples to determine iodine status will also be collected monthly.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTIodine tabletIodine tablets containing 200 ug iodine as potassium iodate
DIETARY_SUPPLEMENTPlacebo tabletPlacebo tablet without iodine

Timeline

Start date
2013-11-01
Primary completion
2014-06-01
Completion
2014-07-01
First posted
2013-11-15
Last updated
2014-07-30

Locations

2 sites across 1 country: Morocco

Source: ClinicalTrials.gov record NCT01985204. Inclusion in this directory is not an endorsement.