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Clinical Trial Summary

This is a double blinded, randomised, crossover study with 12 healthy men between 18 and 40 year. The design is based on 6 days:

- day 1: On day time administration of LPS.

- day 2: On night time administration of LPS.

- day 3: On day time administration of LPS + Placebo.

- day 4: On day time administration of LPS + melatonin.

- day 5: On night time administration of LPS + placebo.

- day 6: On night time administration og LPS + melatonin.

Measuring the inflammatoric and oxidative response of LPS and the effect of melatonin compared to placebo on the endotoxaemia.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01087359
Study type Interventional
Source Herlev Hospital
Contact
Status Completed
Phase Phase 4
Start date June 2010
Completion date February 2011