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Mechanisms of Human Cutaneous Microcirculation in Healthy Volunteers - Article


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Clinical Trial: Mechanisms of Human Cutaneous Microcirculation in Healthy Volunteers

This study is currently recruiting patients.
Verified by University Hospital Angers September 2005

Sponsored by: University Hospital Angers
Information provided by: University Hospital Angers
ClinicalTrials.gov Identifier: NCT00152724

Purpose

Microvascular dysfunctions are criticals events in several diseases including diabetes. This study will develop a methodology for microvascular investigation in human skin.The purpose of the study is to investigate the physiological response of the cutaneous microcirculation to physical, thermal, mechanical or chemical stimulations.
Condition Intervention Phase
Healthy volunteers
 Device: pressure strain system, iontophoresis
 Drug: scopolamin
 Drug: emla
 Drug: capsaicin
 Drug: aspirin
 Drug: clopidogrel
 Drug: celecoxib
 Drug: indomethacin
 Drug: acetylcholine
 Drug: sodium nitroprusside
 Drug: brethyllium
 Device: general and local heating
Phase IV

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Diagnostic, Randomized, Double-Blind, Placebo Control, Parallel Assignment

Official Title: Etude De La Reserve Vasomotrice Microcirculatoire cutanée

Further Study Details: 
Primary Outcomes: Amplitude of the vasomotor response to stimuli
Secondary Outcomes: Kinetics of the vasomotor response to stimuli
Expected Total Enrollment:  85

Study start: January 1996;  Expected completion: January 2007
Last follow-up: January 2007;  Data entry closure: January 2007

This Study has investigated various aspect of the physiology of the microcirculation in the past years and is stil recuiting under parallel protocols of physiological investigations of the neurovascular control of the cutaneous microcirculation

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Healthy volunteers with no clinical signs of, or risk factors for, vascular disease

Exclusion Criteria:

  • Smokers, Pregnancy, Allergy,

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00152724

Pierre ABRAHAM, MD, PhD      (0)2-41-35-46-17  Ext. 33    piabraham@chu-angers.fr

France
      Laboratoire de Physiologie et Explorations Vasculaires - CHU Angers, Angers,  49033,  France; Recruiting
Pierre ABRAHAM, MD, PhD  (0)2-41-35-46-17  Ext. 33    piabraham@chu-angers.fr 

Study chairs or principal investigators

Jean Louis SAUMET, MD - PhD,  Principal Investigator,  University Hospital Angers   

More Information

Publications that report results of this study

Tartas M, Durand S, Koitka A, Bouye P, Saumet JL, Abraham P. Anodal current intensities above 40 microA interfere with current-induced axon-reflex vasodilatation in human skin. J Vasc Res. 2004 May-Jun;41(3):261-7. Epub 2004 May 19.

Durand S, Fromy B, Humeau A, Sigaudo-Roussel D, Saumet JL, Abraham P. Break excitation alone does not explain the delay and amplitude of anodal current-induced vasodilatation in human skin. J Physiol. 2002 Jul 15;542(Pt 2):549-57.

Tartas M, Bouye P, Koitka A, Durand S, Gallois Y, Saumet JL, Abraham P. Early vasodilator response to anodal current application in human is not impaired by cyclooxygenase-2 blockade. Am J Physiol Heart Circ Physiol. 2005 Apr;288(4):H1668-73. Epub 2004 Nov 24.

Durand S, Tartas M, Bouye P, Koitka A, Saumet JL, Abraham P. Prostaglandins participate in the late phase of the vascular response to acetylcholine iontophoresis in humans. J Physiol. 2004 Dec 15;561(Pt 3):811-9. Epub 2004 Oct 21.

Durand S, Fromy B, Tartas M, Jardel A, Saumet JL, Abraham P. Prolonged aspirin inhibition of anodal vasodilation is not due to the trafficking delay of neural mediators. Am J Physiol Regul Integr Comp Physiol. 2003 Jul;285(1):R155-61.

Durand S, Fromy B, Koitka A, Tartas M, Saumet JL, Abraham P. Oral single high-dose aspirin results in a long-lived inhibition of anodal current-induced vasodilatation. Br J Pharmacol. 2002 Oct;137(3):384-90.

Durand S, Fromy B, Bouye P, Saumet JL, Abraham P. Vasodilatation in response to repeated anodal current application in the human skin relies on aspirin-sensitive mechanisms. J Physiol. 2002 Apr 1;540(Pt 1):261-9.

Study ID Numbers:  CP96-04
Last Updated:  September 8, 2005
Record first received:  September 8, 2005
ClinicalTrials.gov Identifier:  NCT00152724
Health Authority: France: Ministry of Health
ClinicalTrials.gov processed this record on 2005-09-13


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Page Updated: November 22, 2004
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