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Effect of Standardized Lacrimal Sac Massage Compared With Probing for Congenital Lacrimal Duct Obstruction

Sun Yat-sen University logo

Sun Yat-sen University

Status

Not yet enrolling

Conditions

Nasolacrimal Duct Obstruction

Treatments

Procedure: Lacrimal sac massage
Procedure: tear duct probing

Study type

Interventional

Funder types

Other

Identifiers

NCT06924723
2025KYPJ036

Details and patient eligibility

About

Congenital nasolacrimal duct obstruction (CNLDO) is a common ophthalmic condition in children, presenting with tearing and pus overflow, with a prevalence of 5%-20% within 1 year of age. Although most cases resolve spontaneously within 1 year of age, some children require treatment. Lacrimal sac massage is a non-invasive, easy and cost-effective conservative treatment that helps to unblock the obstruction by increasing the pressure in the tear duct. Studies have shown that massage has a 93% cure rate in children under 8 months of age. In contrast, tear duct probing is effective but invasive and risky. In recent years, with the development of minimally invasive techniques, lacrimal sac massage has received renewed attention, and studies have shown its efficacy to be comparable to probing. However, there are problems of non-standardized massage timing and techniques in clinical practice, which affects the therapeutic efficacy. This study aims to assess whether the efficacy of standardized dacryocystic massage is not inferior to that of dacryocystorhinostomy through a randomized controlled trial, providing a reference for the treatment of CNLDO.

Enrollment

160 estimated patients

Sex

All

Ages

3 months to 1 year old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age from 3 months to 1 year;
  2. Presence of at least one symptom of CNLDO (tear spillage, mucous discharge) in one or both eyes;
  3. No surgical treatment for NLD (probing, balloon dilation, tube placement, DCR, etc.);
  4. Can cooperate with the examination and subsequent follow-up;
  5. Guardians agreed to be enrolled in the study and signed an informed consent form.

Exclusion criteria

  1. Combination of presenting infections of the conjunctiva and cornea;
  2. Combination of other serious ocular surface and intraocular disorders that may affect the therapeutic effect;
  3. Congenital malformation syndromes, developmental delays, facial anomalies, facial deformities; history of surgery or injury to the lacrimal duct, history of punctal occlusion, history of lacrimal fistula, history of congenital bulging of the lacrimal sac, history of acute dacryocystitis, history of severe blepharitis, and perinatal abnormalities such as preterm labor, low birth weight, and so on;

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

160 participants in 2 patient groups

control subjects
Active Comparator group
Treatment:
Procedure: tear duct probing
experimental group
Experimental group
Treatment:
Procedure: Lacrimal sac massage

Trial contacts and locations

0

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Central trial contact

Xuanwei Liang

Data sourced from clinicaltrials.gov

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