研究目的
To assess the efficacy and safety of femtosecond laser (FL) for patients with myopia systematically.
研究成果
This study will provide a comprehensive evidence summary on FL for patients with myopia, summarizing the latest evidence on assessing efficacy and safety of FL for myopia.
研究不足
The study is based on published studies, and the results are still inconsistent. The heterogeneity among eligible studies may affect the outcome results.
1:Experimental Design and Method Selection:
This study is a systematic review protocol of randomized controlled trials (RCTs) assessing the efficacy and safety of FL for patients with myopia.
2:Sample Selection and Data Sources:
Participants with clinical diagnosis of myopia will be considered for inclusion without any restrictions of race, sex, age, and their economic sources.
3:List of Experimental Equipment and Materials:
RevMan
4:3 software will be utilized for statistical analysis. Experimental Procedures and Operational Workflow:
Systematic literature search from electronic databases up to the present, study selection, data extraction, assessment of risk of bias, missing data management, measurements of treatment effect, assessment of heterogeneity, subgroup analysis, sensitivity analysis, reporting bias, and data synthesis.
5:Data Analysis Methods:
Statistical analysis will be performed using RevMan 5.3 software.
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