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. 2019 Dec 17;2019(12):CD012801. doi: 10.1002/14651858.CD012801.pub2

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.
Participants Baseline characteristics
Toric IOLs
  • Mean age in years (range):  72 (60–79)

  • Sex (% men): not reported

  • Preoperative astigmatism: corneal: 1.39 (range not reported)

  • Preoperative astigmatism: refractive: 1.30 (range not reported)

  • Number of people (eyes): 33 (42)


LRI
  • Mean age in years (range): 73 (60–79)

  • Sex (% men): not reported

  • Preoperative astigmatism: corneal: 1.41 (range not reported)

  • Preoperative astigmatism: refractive: 1.21 (range not reported)

  • Number of people (eyes): 33 (42)


Overall
  • Mean age in years (range): 72 (60–79)

  • Sex (% men): 55%

  • Preoperative astigmatism: corneal:  not reported 

  • Preoperative astigmatism: refractive: not reported

  • Number of people (eyes): 66 (84)


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
Interventions Intervention characteristics
Toric IOLs
  • Type of IOL: Tecnis toric


LRI
  • Type of IOL: Tecnis spherical

  • Incision technique: conventional temporal clarity cornea incision phacoemulsification and spherical IOL implantation combined with LRIs on steep axial position.

Outcomes Visual acuity, corneal astigmatism and refraction
Adverse effects: not reported
Follow‐up: 3 months
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
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.