Clinical Trials Directory

Trials / Completed

CompletedNCT01465646

Bioavailability Investigations of Thyronajod Mite Tablets of Dosage Strengths 50 μg Levothyrox-ine/75 μg Iodine, and 100 μg Levothyroxine/75 μg Iodine vs. a Levothyroxine Drinking-Solution: A Randomised Cross Over Study in Healthy Male Individuals. Currently: 100 μg/ 75 μg Tablets

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Heidelberg University · Academic / Other
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to measure the area under the curve (AUC0-48h; extent of systemic availability) and the maxi-mum concentrations (Cmax) of total serum levothyroxine (TT4, bound and free fraction) after a single pharmacological dose of 600 μg administered as tablets also containing iodine supple-ments vs. the same dose of levothyroxine administered as a reference solution without iodine.

Conditions

Interventions

TypeNameDescription
DRUGlevothyroxine
DRUGlevothyroxine

Timeline

Start date
2003-06-01
Primary completion
2003-12-01
Completion
2003-12-01
First posted
2011-11-07
Last updated
2011-11-07

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01465646. Inclusion in this directory is not an endorsement.