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Comparing three frequencies for phacoemulsification for cataract

Comparison of effective phacoemulsification time and corneal endothelial cell loss using three different ultrasound frequencies in phacoemulsification

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013238
Enrollment
165
Registered
2018-04-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- cataract

Interventions

Intervention1: 53 KHz frequency ultrasound: phacoemulsification using 53KHz Control Intervention1: 28 KHz frequency ultrasound: phacoemulsification using 28 KHz Control Intervention2: 42 KHz frequency

Sponsors

Dr Praveen Kumar Malik
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of age >40 yrs having Grade 4.0-6.9 (LOCS III grading) of senile cataract 2. Patients willing to participate in the study with written consent

Exclusion criteria

Exclusion criteria: 1. Patients with pre-operative endothelial cell density count less than 1500 cells/mm2 . 2. Eyes with any kind of corneal dystrophy or corneal scars preventing visualisation of cataract for reliable grading 3. Raised intraocular pressure ( > 21 mmHg) 4. Previous intraocular surgery

Design outcomes

Primary

MeasureTime frame
EFFECTIVE PHACOEMULSIFICATION TIME Timepoint: Peroperative

Secondary

MeasureTime frame
TOTAL ULTRASOUND TIME Timepoint: PER OPERATIVE;Best Corrected Visual AcuityTimepoint: Preoperatively,1 week, 1 month;Central Corneal Thickness(CCT)Timepoint: Preoperatively,1 week, 1 month,3 months, 6 months ,9 months, 1 year;Coefficient of variation of cell size(CV)Timepoint: Preoperatively,1 week, 1 month,3 months, 6 months ,9 months, 1 year;Endothelial Cell Density(CD)Timepoint: Preoperatively,1 week, 1 month,3 months, 6 months ,9 months, 1 year;Hexagonal Cell Count(6A)Timepoint: Preoperatively,1 week, 1 month,3 months, 6 months ,9 months, 1 year;Intraocular PressureTimepoint: Preoperatively,1 week, 1 month

Countries

India

Contacts

Public ContactDr Nisha Bharti

PGIMER & RMLHospital

tarudewan@hotmail.com9810673180

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026