Actively Recruiting
Reducing Patient Waiting Time for Cataract Surgery
Led by Seva Canada Society · Updated on 2026-04-30
360
Participants Needed
1
Research Sites
35 weeks
Total Duration
On this page
Sponsors
S
Seva Canada Society
Lead Sponsor
D
Divyajyoti Trust - Tejas Eye Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to examine how coordination between hospital departments affects patient flow between the free ward (B1), paid ward (C1) and the operating theatre (OT) for cataract surgeries at a tertiary eye care hospital. This will be an Interventional study using both quantitative and qualitative methods conducted at Tejas Eye Hospital. Patients aged 40-85 years, scheduled for cataract surgery during the study period will be included. Two trained investigators would observe the process and collect the data in structured format from ward admission to transfer into the operating theatre. Every participant would be observed from the ward on the day of his schedule surgery till his surgery is over in operation theatre. Demographic details and personal characteristics of every participant would be recorded in data collection form. In this pathway, timings, events, errors, deviations would be recorded at different spots between ward and operation theatre in first phase of study. Data would be collected from total 364 participants selected using stratified sampling technique. The data will be analyzed using MS excel and EpInfo. Summary statistics would be calculated for different variables and listing of various events and errors would be done. Using the above analysis various delays, communication gaps and different deviation would be identified. A dissemination meeting would be organized with all involved in above processes and findings would be shared in detail. Specific intervention would be decided for execution in the second phase of this study. In second phase, predetermined interventions from analysis of first phase would be implemented and similar data collection would be carried out to see the impact of interventions. Data collection would be done from the phase one sample size and comparison would be carried out for important variables like delays to establish the final outcome of the study. Similarly reduction in frequencies of errors and deviations would also be calculated.
CONDITIONS
Official Title
Reducing Patient Waiting Time for Cataract Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age > 20 years
- Adult cataract surgical patients.
You will not qualify if you...
- Age < 20 years
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Sri Sankaradeva Nethralaya
Guwahati, Assam, India, 781028
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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