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RCT of Evening Primrose Oil for the Treatment of Breastfeeding Pain

S

St. Luke's Hospital, Pennsylvania

Status

Unknown

Conditions

Breast Feeding

Treatments

Dietary Supplement: Evening Primrose Oil
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03876899
SLIR 2018-111

Details and patient eligibility

About

Breastfeeding related mastalgia is a common post-partum complaint. We propose a double-blind, randomized, placebo-controlled trial that investigates the use of Evening Primrose Oil in the treatment of breastfeeding related mastalgia.

Enrollment

80 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • currently breastfeeding
  • recent delivery within the trailing 60 days

Exclusion criteria

  • history of seizure disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups, including a placebo group

Evening Primrose Oil
Active Comparator group
Treatment:
Dietary Supplement: Evening Primrose Oil
Placebo
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

0

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Central trial contact

Richard Vigh, MD; James Anasti, MD

Data sourced from clinicaltrials.gov

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