Improving safety in cataract surgery training using a simulator
E3CAPS: Improvement of the Safety of Care in Cataract Surgery Teaching on Eyesi Simulator: Learning Curve and Impact of Sleep Deprivation on Residents in Ophthalmology
This study is testing whether using a simulator can help new eye doctors learn cataract surgery safely and see how lack of sleep affects experienced doctors' performance.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 2 sites (Nantes and 1 other locations) |
| Trial ID | NCT05722080 on ClinicalTrials.gov |
What this trial studies
This project aims to enhance the safety of cataract surgery by utilizing the EyeSi simulator to model the learning curve of novice ophthalmology residents. The study involves two main axes: the first focuses on training novice residents through supervised sessions to assess their surgical skills over time, while the second evaluates the impact of sleep deprivation on the performance of experienced residents. Participants will undergo standardized assessments to measure their surgical proficiency and cognitive performance under varying conditions. The goal is to establish a 'license to operate' based on demonstrated competency.
Who should consider this trial
Good fit: Ideal candidates include novice and experienced residents in ophthalmology who are undergoing training.
Not a fit: Patients who are not involved in ophthalmology training or who are not residents may not receive any benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved training protocols that enhance the safety and effectiveness of cataract surgeries.
How similar studies have performed: Other studies have shown success in using simulation training for surgical procedures, indicating that this approach is promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Novice resident in Ophthalmology (Axis 1) * Experienced resident in Opthalmology (Axis 2 ) Exclusion Criteria: * N/A
Where this trial is running
Nantes and 1 other locations
- CHU Nantes — Nantes, France (Recruiting)
- CHU Tours — Tours, France (Recruiting)
Study contacts
- Principal investigator: Pierre Lebranchu, M.D — Nantes University Hospital
- Study coordinator: Jean-Baptiste Ducloyer, M.D
- Email: jeanbaptiste.ducloyer@chu-nantes.fr
- Phone: +33 2 53 48 28 57
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.