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Characterization of Local Vascular Effects of LNMMA
This study has been completed.
Sponsored by: Dresden University of Technology
Information provided by: Dresden University of Technology
ClinicalTrials.gov Identifier: NCT00180063
  Purpose

Characterization of an unexpected venodilative effect of higher L-NMMA-doses in dorsal human hand veins.


Condition Intervention
Healthy Subjects
Drug: L-NMMA(drug)

Drug Information available for: omega-N-Methylarginine
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Active Control, Crossover Assignment, Efficacy Study

Further study details as provided by Dresden University of Technology:

Study Start Date: October 2003
Estimated Study Completion Date: September 2005
  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • healthy subjects

Exclusion Criteria:

  • any relevant disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00180063

Locations
Germany
Institute of Clinical Pharmacology, Medical Faculty, University of Technology
Dresden, Germany, 01307
Sponsors and Collaborators
Dresden University of Technology
Investigators
Study Chair: Wilhelm Kirch, MD Institute of Clinical Pharmacology
  More Information

Study ID Numbers: IKPD 01-02 Amend LNMMA
Study First Received: September 9, 2005
Last Updated: November 1, 2005
ClinicalTrials.gov Identifier: NCT00180063  
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Study placed in the following topic categories:
Omega-N-Methylarginine
Healthy

ClinicalTrials.gov processed this record on January 16, 2009