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Engorgement Study With a Double Electric Breast Pump

NCT01619371 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 21

Last updated 2012-06-14

No results posted yet for this study

Summary

The purpose of this study is to analyze the effectiveness of an FDA approved Class II medical device, the Simplisse Double Electric Breast Pump, in relieving the symptoms of engorgement.

Conditions

  • Engorgement

Interventions

DEVICE

Simplisse Double Electric Breast Pump

Use of breast pump for 10 minutes.

Sponsors & Collaborators

  • Foundation for Maternal Infant and Lactation Knowledge

    lead OTHER

Principal Investigators

  • Jimi Francis, MS,PhD,IBCLC · Foundation for Maternal Infant and Lactation Knowledge

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2011-05-31
Completion
2011-05-31

Countries

  • United States

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 NCT01619371 on ClinicalTrials.gov