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NCT02951351 · ClinicalTrials.gov registry record · NA
Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections
A NA study of Pain, Postoperative and Age-related Macular Degeneration, sponsored by Mayo Clinic.
- Completed
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT02951351 is a NA study of Pain, Postoperative and Age-related Macular Degeneration that has completed, run by Mayo Clinic. The registered enrollment target is 36 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02951351, a NA study of Pain, Postoperative and Age-related Macular Degeneration, has completed, sponsored by Mayo Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine.
Conditions Studied
Interventions
- DRUG Proparacaine
- PROCEDURE Conjunctival culture
Study Locations (1)
Minnesota
- Mayo Clinic - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2016-10-12 |
| Est. Completion | 2018-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02951351
The ClinicalTrials.gov registry entry for NCT02951351 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (87% lower). The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Proparacaine is the first listed.
NCT02951351 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT02951351 about?
NCT02951351 is a clinical study titled "Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections". The specific aims of this study are to compare patient experience with and without a proparacaine drop after povidone iodine.
What is the current status of trial NCT02951351?
This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2016-10-12. Estimated completion is 2018-02.
What conditions does trial NCT02951351 study?
This clinical trial studies the following conditions: Pain, Postoperative, Age-related Macular Degeneration, Diabetic Macular Edema, Injection Site Infection, Injection Site.
What interventions are being tested in trial NCT02951351?
The interventions under investigation include: Proparacaine (DRUG), Conjunctival culture (PROCEDURE).
Who is sponsoring clinical trial NCT02951351?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02951351 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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