Comparison of the Effectiveness of drippng breast milk in Infant's Eye and Academic Therapy in Neonates Lacrimal Duct Obstruction

Comparison of the Effectiveness of dripping breast milk in Infant's Eye and Academic Therapy in Neonates Lacrimal Duct Obstruction

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230530058339N1

Enrollment

Registered

2023-09-12

Start date

2023-03-21

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Nazolacrimal obstruction. Neonatal obstruction of unspecified nasolacrimal duct

Interventions

Intervention 1: In the intervention group, the breastfeeding will be dropped to the eye every six hours, and follow-up examinations will be performed every two weeks to one month and then monthly unti

Eligibility

Sex/Gender

All

Age

No minimum to 11 Months

Inclusion criteria

Inclusion criteria: Infants who did not receive any treatment with lacrimal duct obstruction after two weeks No other diagnosis has been considered for them Breastfed babies

Exclusion criteria

Exclusion criteria: Age more than 11 months Using other treatment methods such as probe Development of dacryocystitis Diagnosis of other eye diseases

Design outcomes

Primary

Measure	Time frame
Inflammation. Timepoint: At the beginning of the study and after two weeks and then every month until the inflammation is removed. Method of measurement: questionnaire.;Redness. Timepoint: At the beginning of the study and after two weeks and then every month until the redness is removed. Method of measurement: questionnaire.;Obstruction. Timepoint: At the beginning of the study and after two weeks and then every month until the obstruction is removed. Method of measurement: questionnaire.	—

Measure

Time frame

Inflammation. Timepoint: At the beginning of the study and after two weeks and then every month until the inflammation is removed. Method of measurement: questionnaire.;Redness. Timepoint: At the beginning of the study and after two weeks and then every month until the redness is removed. Method of measurement: questionnaire.;Obstruction. Timepoint: At the beginning of the study and after two weeks and then every month until the obstruction is removed. Method of measurement: questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Amini

Jeeroft University of Medical Sciences

nooraamini30@gmail.com+98 21 2231 4155

Outcome results

None listed

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