Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
NCT07484659

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

Age: 20Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 20 years
  • Adult cataract surgical patients.
Not Eligible

You will not qualify if you...

  • Age < 20 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sri Sankaradeva Nethralaya

Guwahati, Assam, India, 781028

Actively Recruiting

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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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Reducing Patient Waiting Time for Cataract Surgery | DecenTrialz