Surgical Procedure Efficiency Evaluation stuDy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAlcon Research
About this trial
The purpose of this real-world evidence study is to compare surgical procedure times for UNITY® VCS and CONSTELLATION® Vision System.
Eligibility criteria
Qualifiers
Able to understand and sign an informed consent form (ICF) that has been approved by an ethics committee.
Planned combined phacovitrectomy procedure at one of the selected surgical sites.
Planned combined phacovitrectomy procedure with 25-gauge (G) vitrectomy tools.
Disqualifiers
Unplanned/emergency phacovitrectomy.
Pregnant.
Past history of phacovitrectomy. cataract, vitrectomy in the planned operative eye.
Other protocol-defined exclusion criteria may apply.
Trial design
Treatments tested in this trial
- UNITY VCS
- CONSTELLATION
Treatment groups
180 Participants
are divided into 2 treatment groupsSponsors and collaborators
Alcon Research
Lead sponsor
Manchester Royal Eye Hospital
Collaborator
Source ClinicalTrials.gov