Actively Recruiting
Reducing Patient Waiting Time for Cataract Surgery Through Improved Coordination Between Ward and Operation Theatre
Led by Seva Canada Society · Updated on 2026-04-30
360
Participants Needed
1
Research Sites
8 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
Researchers are investigating how coordination between hospital departments affects patient flow during cataract surgeries at a tertiary eye care hospital. The study focuses on the movement of patients between the free ward, paid ward, and operating theatre. It aims to identify delays, communication gaps, and errors that occur during the process, which are common challenges in healthcare settings and can impact patient safety and satisfaction. This interventional study is conducted in two phases at Tejas Eye Hospital. In the first phase, trained investigators observe and record detailed data on patient movement and communication from ward admission to surgery completion. The second phase involves implementing specific interventions based on the first phase findings to improve coordination, followed by similar data collection to assess the impact on waiting times and errors. Participants will be adults aged over 20 years scheduled for cataract surgery. Researchers collect demographic data, timing of events, errors, and patient satisfaction information. The main measurement is the waiting time from ward call-up to entry into the operating theatre. Data analysis includes summary statistics and comparison of delays and communication issues before and after interventions. The study will last at least six months, with close monitoring of patient flow and workflow improvements.
CONDITIONS
Brief 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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of scheduled surgery
Participants undergo cataract surgery with improved coordination between the ward and operating theatre using standardized procedures to reduce waiting time.
1 in-person visit on the day of surgery
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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