Clinical Trials Directory

Trials / Completed

CompletedNCT01070940

L-NMMA Dose-response Study in Healthy Subjects

L-NMMA's Effect on Renal and Cardiovascular Variables in Healthy Subjects. A Randomized, Placebo-controlled Crossover Study.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Regional Hospital Holstebro · Academic / Other
Sex
Male
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to investigate the effect of different levels of nitric oxide inhibition on blood pressure and arterial stiffness in healthy subjects. L-NMMA, an inhibitor of the nitric oxide synthase, is administered as bolus injection followed by continuous infusion, and is expected to raise blood pressure and arterial stiffness according to L-NMMA dose.

Conditions

Interventions

TypeNameDescription
DRUGNG-monomethyl-L-arginine (L-NMMA)3 mg/kg IV priming dose + 2 mg/kg/hr IV infusion for 1 hour
DRUGNG-monomethyl-L-arginine (L-NMMA)6 mg/kg IV priming dose + 4 mg/kg/hr IV infusion for 1 hour
DRUGNG-monomethyl-L-arginine (L-NMMA)4.5 mg/kg IV priming dose + 3 mg/kg/hr IV infusion for 1 hour
DRUGPlaceboIsotonic saline solution IV priming dose + IV infusion for 1 hour

Timeline

Start date
2010-02-01
Primary completion
2010-06-01
Completion
2010-06-01
First posted
2010-02-18
Last updated
2011-02-21

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01070940. Inclusion in this directory is not an endorsement.