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NCT01300949 · ClinicalTrials.gov registry record · NA

Spaeth/Richman Contrast Sensitivity Test

A NA study, sponsored by Wills Eye.

Completed
Registry status
NA
Development phase
314
Enrollment target

NCT01300949 is a NA study that has completed, run by Wills Eye. The registered enrollment target is 314 participants.

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The verdict

NCT01300949, a NA study, has completed, sponsored by Wills Eye.

COMPLETED
Registry status
NA
Development phase
314 participants
Enrollment target

Study Summary

The Spaeth-Richman Contrast Sensitivity (SPARCS) test is a new method of assessing contrast sensitivity. The test, another way to measure vision, is performed on any standard computer with internet access. Patients will be tested with SPARCS and with the standard Pelli-Robson contrast test.

Interventions

  • DIAGNOSTIC_TEST Spaeth/Richman Contrast Sensitivity Test
  • DIAGNOSTIC_TEST Pelli-Robson Contrast Sensitivity Chart

Trial Details

FieldValue
Enrollment Target 314 participants
Start Date 2010-01
Est. Completion 2014-04
Phase NA

Sponsor

Wills Eye

59 total trials

What the Registry Record Tells You About NCT01300949

The ClinicalTrials.gov registry entry for NCT01300949 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 314 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wills Eye, which has 59 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Spaeth/Richman Contrast Sensitivity Test is the first listed.

NCT01300949 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01300949 about?

NCT01300949 is a clinical study titled "Spaeth/Richman Contrast Sensitivity Test". The Spaeth-Richman Contrast Sensitivity (SPARCS) test is a new method of assessing contrast sensitivity. The test, another way to measure vision, is performed on any standard computer with internet access. Patients will be tested with SPARCS and with the standard Pelli-Robson contrast test.

What is the current status of trial NCT01300949?

This trial is currently completed. It is a NA study. The enrollment target is 314 participants. The study started on 2010-01. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01300949?

The interventions under investigation include: Spaeth/Richman Contrast Sensitivity Test (DIAGNOSTIC_TEST), Pelli-Robson Contrast Sensitivity Chart (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT01300949?

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

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.