Last updated: January 17, 2024
Sponsor: Instituto de Oftalmología Fundación Conde de Valenciana
Overall Status: Active - Recruiting
Phase
1
Condition
N/ATreatment
Dacryocystorhinostomy and amniotic membrane
Conventional dacryocystorhinostomy
Clinical Study ID
NCT06226181
CI-028-2017
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients over 18 years old
- Diagnosis of Nasolacrimal Duct Obstruction or Score ≥ 2 on the Munk Scale
- Patients able to undergo general anesthesia
- Patients able to keep follow-up
- Patients willing to participate in the study and signed informed consent
Exclusion
Exclusion Criteria:
- Patients with ocular surface diseases that affect surgical outcomes, such asblepharitis, lacrimal punctum epithelization, kissing punctae, facial nerve palsy,allergic conjunctivitis, etc
- Patients with eyelid malpositions
- Patients diagnosed with systemic inflammatory diseases, such as granulomatosis withpolyangiitis, sarcoidosis, etc
- Previous history of facial trauma with nasal bone fractures
- Pregnancy and lactation
Study Design
Total Participants: 32
Treatment Group(s): 2
Primary Treatment: Dacryocystorhinostomy and amniotic membrane
Phase: 1
Study Start date:
January 01, 2024
Estimated Completion Date:
March 01, 2025
Study Description
Connect with a study center
Institiuto de Oftalmología Fundación Conde de Valenciana
Mexico City, 06800
MexicoActive - Recruiting
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