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Clinical Trials/NCT01092156
NCT01092156
Completed
Not Applicable

Prenatal Breastfeeding Education to Reduce Nipple Pain

University of California, Davis1 site in 1 country200 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nipple Pain During Lactation
Sponsor
University of California, Davis
Enrollment
200
Locations
1
Primary Endpoint
Nipple pain day 3 postpartum
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This study is a randomized controlled trial to evaluate the effectiveness of different approaches to prenatal teaching of infant latch.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
November 2008
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pregnant women who intend to breastfeed their infants
  • Single infant
  • Resides in catchment area
  • Has phone
  • Speaks English

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Nipple pain day 3 postpartum

Time Frame: Day 3 postpartum

Secondary Outcomes

  • Breastfeeding status day 30 postpartum(Day 30 postpartum)

Study Sites (1)

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