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Dafilon® Suture Material in Patients Undergoing Ophthalmic Surgery — OPHTHADA  

Eye Diseases Clinical Trial

Official title:
Observational, Retrospective Clinical Study in Patients Undergoing Ophthalmic Surgery Using Dafilon® Suture Material (Dafilon® USP (United States Pharmacopeia) Sizes From 8/0 to 11/0)

Clinical Trial Summary

This is an observational, retrospective postmarket clinical follow-up study and includes all patients who underwent any ophthalmic surgery using Dafilon® suture in the selected centres between 2018 and 2020, therefore no sample size can be given but the planned sample size shall be at least 200 eyes (around 100 patients depending on the number of operated eyes per patient) to conduct meaningful subgroup analysis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05968443
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date January 8, 2019
Completion date May 10, 2022
View Details
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