Dong 2015.
Methods |
Study design: randomised controlled trial Study grouping: parallel group Eyes/people: 1 or 2 eyes per person, unclear how the eyes were selected and whether analysed adjusted for within‐person correlation. |
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Participants |
Baseline characteristics Toric IOLs
LRI
Overall
Inclusion criteria: aged ≥ 60 years; diagnosed senile cataract before surgery; pupils of normal round shape and diameter > 3 mm; hardness of lens nuclear categorised according LOCS – from II to IV level; regular corneal astigmatism within range 1.5–4.0 D. Exclusion criteria: people with retinal disease, glaucoma, keratitis, irregular corneal astigmatism, recent acute eye infections, pterygium; history of ocular trauma and surgical procedure. Pretreatment differences: none reported |
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Interventions |
Intervention characteristics Toric IOLs
LRI
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Outcomes | Visual acuity, corneal astigmatism and refraction Adverse effects: not reported Follow‐up: 3 months |
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Identification |
Sponsorship source: not reported Country: China Authors name: Yong‐Xiao Dong Email: 187299703@qq.com Conflict of interest: not reported Trial registration ID: not reported Date study conducted: not reported |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Judgement comment: random allocation done using random number table. |
Allocation concealment (selection bias) | Unclear risk | Judgement comment: information not provided. We contacted study authors for clarification but received no response. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Judgement comment: information not provided. We contacted study authors for clarification but received no response. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Judgement comment: information not provided. We contacted study authors for clarification but received no response. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Judgement comment: no description of participants who withdrew or were lost to follow‐up. We contacted study authors for clarification but received no response. |
Selective reporting (reporting bias) | Unclear risk | Judgement comment: no access to protocol or trial registration entry. We contacted study authors for clarification but received no response. |