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Drug Excretion in Breast Milk

Drug Excretion in Breast Milk

This study explores how medications enter breast milk, which is not yet fully understood. We will investigate this process using the medication cimetidine, an over-the-counter heartburn medication that is safe for use while breastfeeding and has few side effects.

Participants will give consent during pregnancy, but all study activities will occur after delivery.

Participation in the study involves three separate study days, each lasting 12-13 hours. These days will be scheduled at 3-5 weeks, 3-4 months, and 6-8 months postpartum. On each study day, participants will take a single dose of cimetidine and provide samples of blood, urine, and breast milk. Participants are welcome to bring their infants to the study days.

Participants who complete all study procedures will receive $700 in compensation.

Participant Eligibility

Inclusion Criteria:
Between the ages of 18-50 years old
Generally healthy
Planning to lactate for at least six months postpartum
Able to provide written informed consent

Exclusion Criteria:
Multiple gestation (twins, triplets, etc.)
Hypersensitivity to cimetidine
Receiving medication(s) known to interact with cimetidine
Known kidney disease
Known liver disease
Inability to fast for 4 hours prior to the study
Use of tobacco or other nicotine containing products

Contact

Madison Navarro
(206) 543-5600

Additional Study Details

Full Study Title
Drug Excretion in Breast Milk

Study ID: STUDY00018397
Start Date: 07/25/2023
End Date: 09/30/2028

Investigator(s)
Dr. Mary Hebert, PharmD, FCCP
Dr. Joanne Wang, PhD
Dr. Emily Fay, MD

Accepts Healthy Volunteers?
Yes

Study Site(s)

University of Washington

1959 NE Pacific St
Seattle, Washington 98195



Interested?

Use the link below to send a message to the study coordinator, or call the number above to speak directly with a study representative.

I am interested in this research study.

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