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User Evaluation in Healthy Volunteers to Verify no Pelvic Floor Contraction is Stimulated When the Modified Neurotech Vital Device is Used Compared to the Neurotech Vital Device

NCT01614730 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2012-07-09

No results posted yet for this study

Summary

This user evaluation study is to verify that the Modified Neurotech Vital Device does not stimulate the pelvic floor muscles compared with the Neurotech Vital Device.

Conditions

  • Contraction of Pelvic Floor Muscle Using EMS

Interventions

DEVICE

Modified Neurotech Vital Device

verify no contraction is stimulated in the Modified Neurotech Vital.

DEVICE

Neurotech Vital Device

Checking there is a contraction of the pelvic floor muscle when the treatment is administered with the Neurotech Vital Device

Sponsors & Collaborators

  • Bio-Medical Research, Ltd.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2012-06-30
Completion
2012-07-31

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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 NCT01614730 on ClinicalTrials.gov