Registry for cataract surgery using phacoemulsification
Registry of PHAcoemulsification for Cataract Surgery
This study is trying to collect and look at data from cataract surgeries using a specific machine to see how new technology affects surgery success and recovery for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100000 (estimated) |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris) |
| Trial ID | NCT06659419 on ClinicalTrials.gov |
What this trial studies
This study aims to establish a nationwide registry to collect and analyze intraoperative data from cataract surgeries performed with the Centurion phacoemulsifier. It will focus on parameters such as ultrasound time, energy delivered, and total surgery duration, among others. The goal is to assess the impact of technological advances on surgical efficiency and patient outcomes. Data will be retrospectively analyzed from at least 100,000 procedures across France, providing valuable insights into the effectiveness of different surgical settings.
Who should consider this trial
Good fit: Ideal candidates for this study are patients undergoing cataract surgery with the Centurion phacoemulsifier.
Not a fit: Patients with complicated surgeries or those whose centers oppose data collection may not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could lead to improved cataract surgery techniques and better patient outcomes through optimized use of phacoemulsification technology.
How similar studies have performed: While there is limited data on similar registries, the approach of collecting large-scale intraoperative data is promising and could provide valuable insights into surgical practices.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- All procedures recorded in Centurions (200 machines). Exclusion Criteria: * Opposition of the center to data collection. * Complicated surgery (e.g. anterior vitrectomy) identified as such in the event log
Where this trial is running
Paris
- Ophthalmology department - Cochin Hospital — Paris, France (Recruiting)
Study contacts
- Principal investigator: Antoine BREZIN, MD, PhD — Assistance Publique - Hôpitaux de Paris
- Study coordinator: Antoine BREZIN, MD, PhD
- Email: antoine.brezin@aphp.fr
- Phone: 01 58 41 22 01
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.