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NCT02477605 · ClinicalTrials.gov registry record · NA
Clinical Comparison of 27+® and 23-gauge ULTRAVIT® 7500 Cpm Vitrectomy Outcomes
A NA study, sponsored by Alcon Research.
- Completed
- Registry status
- NA
- Development phase
- 137
- Enrollment target
NCT02477605 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 137 participants.
The verdict
NCT02477605, a NA study, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 137 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the treatment day change between immediate postoperative and immediate preoperative intraocular pressure (IOP) between 27-gauge and 23-gauge vitrectomy instruments.
Interventions
- DEVICE CONSTELLATION® 27-gauge Combined Surgical Pak
- DEVICE CONSTELLATION® 23-gauge Combined Surgical Pak
- PROCEDURE Vitrectomy surgery
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 137 participants |
| Start Date | 2015-07-16 |
| Est. Completion | 2016-08-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02477605
The ClinicalTrials.gov registry entry for NCT02477605 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 137 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which CONSTELLATION® 27-gauge Combined Surgical Pak is the first listed.
NCT02477605 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02477605 about?
NCT02477605 is a clinical study titled "Clinical Comparison of 27+® and 23-gauge ULTRAVIT® 7500 Cpm Vitrectomy Outcomes". The purpose of this study is to compare the treatment day change between immediate postoperative and immediate preoperative intraocular pressure (IOP) between 27-gauge and 23-gauge vitrectomy instruments.
What is the current status of trial NCT02477605?
This trial is currently completed. It is a NA study. The enrollment target is 137 participants. The study started on 2015-07-16. Estimated completion is 2016-08-31.
What interventions are being tested in trial NCT02477605?
The interventions under investigation include: CONSTELLATION® 27-gauge Combined Surgical Pak (DEVICE), CONSTELLATION® 23-gauge Combined Surgical Pak (DEVICE), Vitrectomy surgery (PROCEDURE).
Who is sponsoring clinical trial NCT02477605?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
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