CompletedNot Applicable

Engorgement Study With a Double Electric Breast Pump

United States21 participantsStarted 2011-03

Plain-language 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.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * first week postpartum seeking lactation management assistance for engorgement, identified as clinically engorged by health care practitioner. Exclusion Criteria: * greater than one week postpartum * less than 18 years of age * non-English speakers * not willing to use double electric breast pump

What they're measuring

Engorgement Relief

Timeframe: 10 minutes per subject

Trial details

NCT IDNCT01619371

SponsorFoundation for Maternal Infant and Lactation Knowledge

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2011-05

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