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Cutaneous Iontophoresis of Iloprost and Treprostinil in Healthy Volunteers

NCT01082484 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2011-10-06

No results posted yet for this study

Summary

The purpose of this study is to test whether prostacyclin analogues' cathodal iontophoresis induce a cutaneous vasodilation in healthy volunteers's forearm, without local side effects.

Conditions

  • Healthy

Interventions

DRUG

treprostinil

Cutaneous iontophoresis at 20 microA/ 100 microA during 20 min

DRUG

iloprost

Cutaneous iontophoresis at 20 microA/ 100 microA during 20 min

DRUG

NaCl 0.9%

Cutaneous iontophoresis at 20 microA/ 100 microA during 20 min

Sponsors & Collaborators

  • University Hospital, Grenoble

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2011-01-31
Completion
2011-01-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01082484 on ClinicalTrials.gov