A Study to Test the Tolerability of an Investigational Electroporation Device in Healthy Adults (V930-001)

Merck Sharp & Dohme (MSD)

Status and phase: Completed; Phase 1

Conditions: Healthy

Treatments: Biological: V930

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00721461

2008_537

V930-001

Details and patient eligibility

About

A study to evaluate the tolerability of electrostimulation applications with an investigational device known as the MedPulser DDS.

Enrollment: 24 patients

Sex: All

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Must be between the ages of 18 and 35
• Woman who are able to become pregnant must use an acceptable form of birth control

Exclusion criteria

• You are breast feeding
• You have taken any type of pain reliever within 12 hours of electrostimulation
• You have participated in another clinical study within 4 weeks of starting this study or plan to participate in another clinical study while participating in this study
• You have muscle atrophy, weakness or neuromuscular disorder

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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24 participants in 1 patient group

1

Experimental group

Description:

V930

Treatment:

Biological: V930