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NCT03038048 · ClinicalTrials.gov registry record · NA

30g vs 33g Needle for Intravitreal Injections

A NA study of Age-related Macular Degeneration and Diabetic Macular Edema, sponsored by Wills Eye.

Completed
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT03038048 is a NA study of Age-related Macular Degeneration and Diabetic Macular Edema that has completed, run by Wills Eye. The registered enrollment target is 50 participants, below the 1,507-participant average among 74 other Age-related Macular Degeneration trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03038048, a NA study of Age-related Macular Degeneration and Diabetic Macular Edema, has completed, sponsored by Wills Eye.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

We are comparing the patient experience between the standard 30 g needle to the smaller 33 g needle for intravitreal injections of ranabizumab or aflibercept for age related macular degeneration, diabetic macular edema, or retina vein occlusions.

Interventions

  • PROCEDURE Varying needle size with intravitreal ranibizumab or aflibercept

Study Locations (1)

Pennsylvania

  • Mid Atlantic Retina- Wills Eye Hospital - Philadelphia

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2017-01-27
Est. Completion 2017-04-27
Phase NA

Sponsor

Wills Eye

59 total trials

What the Registry Record Tells You About NCT03038048

The ClinicalTrials.gov registry entry for NCT03038048 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,507-participant average among 74 other Age-related Macular Degeneration trials with a reported enrollment target (97% lower). The listed sponsor is Wills Eye, which has 59 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Age-related Macular Degeneration appearing as the primary indexed condition, and to 1 intervention - of which Varying needle size with intravitreal ranibizumab or aflibercept is the first listed.

NCT03038048 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT03038048 about?

NCT03038048 is a clinical study titled "30g vs 33g Needle for Intravitreal Injections". We are comparing the patient experience between the standard 30 g needle to the smaller 33 g needle for intravitreal injections of ranabizumab or aflibercept for age related macular degeneration, diabetic macular edema, or retina vein occlusions.

What is the current status of trial NCT03038048?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2017-01-27. Estimated completion is 2017-04-27.

What conditions does trial NCT03038048 study?

This clinical trial studies the following conditions: Age-related Macular Degeneration, Diabetic Macular Edema, Retinal Vein Occlusion.

What interventions are being tested in trial NCT03038048?

The interventions under investigation include: Varying needle size with intravitreal ranibizumab or aflibercept (PROCEDURE).

Who is sponsoring clinical trial NCT03038048?

This trial is sponsored by Wills Eye, which has 59 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03038048 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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