Geneva, April 20 -- International Clinical Trials Registry received information related to the study (ChiCTR2600121848) titled 'Analysis of Postoperative Clinical Efficacy and Visual Quality of VisuMax 800 Femtosecond System SMILEpro' on April 3.
Study Type: Interventional study
Study Design:
Single arm
Primary Sponsor: Hainan Optometry and Ophthalmology Hospital
Condition:
Refractive Error
Recruitment Status: Recruiting
Phase: N/A
Date of First Enrollment: 2026-04-04
Target Sample Size: Experimental group:300;
Countries of Recruitment:
China
To know more, visit https://www.chictr.org.cn/showproj.html?proj=313692
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