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Search / Trial NCT05333939

Moringa Supplementation for Improved Milk Output

Launched by UNIVERSITY OF KENTUCKY · Apr 11, 2022

Trial Information

Current as of May 03, 2025

Completed

Keywords

Maternal And Child Health

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Mom
  • YES:
  • willing to breastfeed or pump for one week
  • willing to complete study activities (at minimum measure 24 hour pumped volume at start and end of capsules, take capsules daily, and answer questions)
  • has access to breastpump (in hospital and/or home)
  • English speaking
  • 18 years or older
  • Gave birth between 2-6 weeks prior to study start
  • NO:
  • taking metoclopramide (trade name Reglan) currently or within 2 weeks of enrollment
  • taking moringa regularly or within 2 weeks of enrollment
  • breast surgery (amplification, reduction, or other)
  • breast condition: Insufficient Glandular tissue
  • unprescribed or street drug use at any point in pregnancy, or enrolled in rehab program or receiving addiction therapy
  • refuses to take 4 capsules twice daily within 2 days of study start
  • wishes to withdraw within 2 days of study start
  • Infant
  • YES:
  • 28-36 and 7 weeks gestation (ie 37 weeks is too old)
  • 2-6 weeks old
  • singleton birth
  • NO:
  • · any condition where breastmilk is clinically contraindicated

About University Of Kentucky

The University of Kentucky is a leading academic institution dedicated to advancing healthcare through innovative research and clinical trials. With a strong emphasis on interdisciplinary collaboration, the university leverages its extensive resources and expertise to conduct rigorous clinical studies aimed at improving patient outcomes and addressing pressing medical challenges. The institution is committed to ethical research practices and strives to enhance community health by translating scientific discoveries into effective treatments and interventions. Through its Clinical Trials Office, the University of Kentucky fosters a supportive environment for researchers and participants alike, ensuring a comprehensive approach to clinical research that meets the highest standards of excellence.

Locations

Lexington, Kentucky, United States

Lexington, Kentucky, United States

Patients applied

0 patients applied

Trial Officials

Suzanna Attia, MD

Principal Investigator

University of Kentucky

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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