Engorgement Study With a Double Electric Breast Pump

N/ACompletedNCT01619371

Foundation for Maternal Infant and Lactation Knowledge21 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Engorgement

Interventions

Simplisse Double Electric Breast PumpDEVICE

Use of breast pump for 10 minutes.

Eligibility

Sex: FEMALEMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

Newborn Care Center Clinic

Reno, Nevada, United States

Outcomes

Primary Outcomes

Engorgement Relief

Relief of engorgement as measured by the engorgement scale.

Time frame: 10 minutes per subject

Data from ClinicalTrials.gov

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