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Facelift Randomized Controlled Trials Compliance With CONSORT Checklist: A Systematic Review
Randomized controlled trials (RCTs) in facelift surgery have poor reporting quality, impacting evidence for facial rejuvenation. Improving trial transparency through pre-registration and protocol publication is crucial for reliable results.
Area of Science:
- Plastic Surgery
- Evidence-Based Medicine
- Clinical Trial Methodology
Background:
- Randomized controlled trials (RCTs) in facelift surgery are limited and inconsistently reported.
- Transparent and reproducible methods are essential for evaluating facelift surgery efficacy and safety.
Purpose of the Study:
- To assess the methodological quality and reporting standards of facelift RCTs.
- To identify adherence patterns and areas for improvement using Consolidated Standards of Reporting Trials (CONSORT) and CONSORT-NPT guidelines.
Main Methods:
- A PRISMA-guided systematic review of facelift RCTs was conducted.
- Methodological quality was assessed using CONSORT 2010/CONSORT-NPT 2017 checklists.
- Risk of bias and evidence quality were evaluated using Cochrane RoB 2.0 and GRADE.
Main Results:
- Ten RCTs (n=457) were included, with mean CONSORT adherence of 56%.
- High adherence was noted for intervention description and statistical analysis, but poor for trial registration and protocol publication.
- Only 3 trials had low risk of bias, with largely low-moderate GRADE certainty.
Conclusions:
- Facelift RCTs exhibit variable and suboptimal reporting, weakening the evidence base for facial rejuvenation.
- Enhancing trial quality necessitates pre-registration, protocol publication, validated outcomes, and CONSORT adherence.
- Standardized reporting and minimum datasets are recommended to strengthen evidence in facial rejuvenation surgery.
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