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comparison of the effect of ostrich oil with breast milk on the improvement of breast fissures in primiparous lactating women

comparison of the effect of ostrich oil with breast milk on the improvement of breast fissures in primiparous lactating women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230204057319N1
Enrollment
106
Registered
2023-05-09
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast fissures. Cracked nipple associated with pregnancy, the puerperium, and lactation

Interventions

Intervention 1: Intervention group: Ostrich oil group: It is a natural oil that is extracted from ostrich fat (tallow) and has significant biological activities in preventing all kinds of pains and in

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: First pregnancy and term Having a breast fissures and scoring at least 3 on the Storr scale be Iranian At least be able to read and write. singleton pregnancy Exclusive breastfeeding The mother is not addicted to smoking or drugs The mother does not have a history of known chronic diseases such as high blood pressure, diabetes, asthma, weakening the immune system, etc Do not have a history of allergy to drugs of animal origin. The mother's absence of nipple abnormalities or previous nipple or areola surgeries Mother's absence of diseases and mental disorders

Exclusion criteria

Exclusion criteria: Puerperal fever or breast infection Infant oral infection Short frenulum of the baby's tongue Possible allergy to ostrich oil cream The mother's use of other treatments Not using ostrich oil for a day or more Not using breast milk for a day or more Using a bottle, breast pump or breast connector during the study Unwillingness to continue participating in the study

Design outcomes

Primary

MeasureTime frame
The pain. Timepoint: The first day (before the intervention), the third day (during the intervention) and the seventh day (end of the intervention). Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Nipple damage. Timepoint: The first day (before the intervention), the third day (during the intervention) and the seventh day (end of the intervention). Method of measurement: Visual analog scale to evaluate pain intensity and Storr scale to evaluate nipple injury severity.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasumeh Koshki

Shahid Beheshti University of Medical Sciences

masumehkoshki1355@gmail.com+98 66 3342 6857

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026