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The effect of Lanolin, Peppermint and Dexpanthenol on traumatic nipple in lactating mothers

Comparing the effect of Lanolin, Peppermint and Dxpanthenol on treatment of traumatic nipple in lactating mothers: a randomized double-blind controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201403116709N16
Enrollment
126
Registered
2014-10-06
Start date
2014-05-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Cracked nipple. Other disorder of breast

Interventions

Intervention 1: Control group: Lanolin cream with trade name of Lanolin made by Iran Nazhoo Company, containing purest Lanolin and no preservative and any other additives that for 2 weeks 3 times a
Treatment - Drugs
Control group: Lanolin cream with trade name of Lanolin made by Iran Nazhoo Company, containing purest Lanolin and no preservative and any other additives that for 2 weeks 3 times a day immediately
Intervention group 1: Peppermint cream, made by pharmacy faculty in Tabriz, containing Carbopol, Methyl paraben, Tritanolamin and Glycerin with 0.2% Peppermint oil added to it that for 2 weeks, 3 tim
Intervention group 2: Dexpanthonel cream with trade name of Panthoderm made by Caspian Company, containing Pantothenic acid for 2 weeks 3 times a day immediately after milking, the amount of the dr

Sponsors

Research dupty of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: single birth; exclusive breastfeeding; term infant; infants less than 2 months of age; earn a minimum score 1 on a scale of NTS and NSRS; mother's lack of sensitivity to Lanolin, Peppermint and Dexpanthenol; 2500-4000 grams birth weight; the absence of abnormal nipple (flat, depressed). Exclusion criteria: infant with tongue and teeth abnormalities; baby use pacifier, glass and plastic nipple; mother with history of mental illness

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Nipple trauma injury. Timepoint: Before the intervention and two weeks after intervention. Method of measurement: Champion scale.

Secondary

MeasureTime frame
Nipple pain. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: pain Sttor scale.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactkazhal Masoudin

Tabriz University of Medical Sciences

K_masoudin@yahoo.com+98 41 1447 4467

Outcome results

None listed

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