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The Effect of Lactation Cookies on Breastfeeding Outcomes in Lactating Women

NCT07030491 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2025-06-22

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if eating lactation cookies can help breastfeeding women make more milk. The main questions it aims to answer are:

* Do lactation cookies help increase milk production?
* Do lactation cookies make the breastfeeding experience easier or better?

Researchers will compare lactation cookies to regular cookies to see if lactation cookies work better.

Participants will:

* Eat 2 cookies every day for 30 days
* Visit the clinic 2 times, at the start and end of the study
* Keep a simple record of their breastfeeding and cookie eating

Conditions

  • Breastfeeding

Interventions

OTHER

Lactation Cookies

Participants will consume 2 cookies per day (approximately 40g daily) for 30 consecutive days. The lactation cookies contain ingredients commonly believed to enhance milk production, including moringa, fenugreek, and ginger.

OTHER

Control Cookies

Participants in the control group will consume 2 cookies per day (approximately 40g total) for 30 consecutive days. These cookies are matched in taste, appearance, and caloric content but do not contain any known galactagogue ingredients.

Sponsors & Collaborators

  • Keserwan Medical Center

    collaborator OTHER

  • Little Melly

    collaborator INDUSTRY

  • Notre Dame University - Louaize

    lead OTHER

Principal Investigators

  • Jessy El Hayek, PhD · Notre Dame University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-06-25
Primary Completion
2025-09-25
Completion
2025-09-25

Countries

  • Lebanon

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 NCT07030491 on ClinicalTrials.gov