Engorgement Study With a Double Electric Breast Pump

Foundation for Maternal Infant and Lactation Knowledge

Status: Completed

Conditions: Engorgement

Treatments: Device: Simplisse Double Electric Breast Pump

Study type: Observational

Funder types: Other

Identifiers

NCT01619371

2614

Details and patient eligibility

About

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.

Enrollment: 21 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

21 participants in 1 patient group

Lactating women

Description:

Lactating women willing to use a breast pump.

Treatment:

Device: Simplisse Double Electric Breast Pump