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临床试验/CTRI/2026/01/101507
CTRI/2026/01/101507尚未招募不适用

Comparative outcomes of toric intraocular lens (IOL) implantation using ALLY-guided workflow versus ZEISS CALLISTO eye markerless guidance in phacoemulsification cataract surgery: a prospective randomized controlled trial

Ministry of Defence1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2026年1月28日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
110
试验地点
1

研究概览

简要总结

Precise alignment of toric intraocular lenses is critical for effective correction of corneal astigmatism during cataract surgery, as each degree of postoperative misalignment can reduce astigmatic correction by approximately 3.3percent. This prospective, randomized controlled trial compares the clinical outcomes of toric IOL implantation using two advanced intraoperative guidance systems: the ALLY femtosecond-assisted workflow and the ZEISS CALLISTO eye markerless guidance. The study aims to evaluate refractive accuracy, rotational stability, surgical efficiency, and patient-reported outcomes following phacoemulsification cataract surgery.

Eligible participants are adults with regular corneal astigmatism more than 1.00 D and visually significant cataracts. Subjects are randomized to receive toric IOL alignment via either ALLY or CALLISTO guidance, with standardized preoperative planning, surgical technique, and postoperative care across both arms. The primary endpoint is  proportion of eyes within 0.50 D and 1.00 D of refractive targets, mean absolute residual refractive cylinder at 3 months postoperatively. Secondary endpoints include IOL rotational stability, uncorrected and corrected distance visual acuity, vector analysis of astigmatism (Alpins method), intraoperative metrics, need for IOL repositioning, patient-reported visual quality, and safety outcomes. Outcome assessors are masked to group allocation, and analyses will be conducted on an intention to treat basis with per protocol sensitivity.

This trial will provide high-quality evidence to inform best practices in toric IOL alignment and may influence future adoption of integrated femtosecond platforms versus markerless image guided systems in cataract surgery

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
40.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Regular corneal astigmatism more than 1.00D (K readings compatible with toric IOL range) Clear corneal media for accurate imaging and aberrometry.

排除标准

  • Irregular astigmatism (topographic evidence), keratoconus or ectasia suspects.
  • Prior corneal or refractive surgery Zonulopathy, pseudoexfoliation with significant instability, traumatic cataract.
  • Corneal opacity, pterygium , severe dry eye Uveitis, uncontrolled glaucoma, macular pathology limiting VA , optic neuropathy.
  • Intraoperative complications precluding planned IOL implantation or axis alignment.

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Sanjay Kumar Mishra

Army Hospital Research and Referral

研究点 (1)

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