Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01476644 · ClinicalTrials.gov registry record · NA

How Has Glaucoma Affected Your Quality of Life?

A NA study, sponsored by Wills Eye.

Completed
Registry status
NA
Development phase
161
Enrollment target

NCT01476644: Completed NA study, sponsored by Wills Eye.

NCT01476644 is a NA study that has completed, run by Wills Eye. The registered enrollment target is 161 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01476644, a NA study, has completed, sponsored by Wills Eye.

COMPLETED
Registry status
NA
Development phase
161 participants
Enrollment target

Study Summary

Hypothesis 1: Self-reported health-related quality of life decreases as vision impairment worsens in subjects with glaucoma. Hypothesis 2: Changes in health-related quality of life are associated with changes in clinical measures of vision and performance-based measures of visual function.

Primary Outcome

National Eye Institute Visual Function-25 questionnaire (NEI VFQ-25) is a measurement of patients perception of their visually related quality of life. Patients select answers from multiple choice lists of responses. Values are re-coded and converted to a scale of 0 to 100 where 0 is extreme difficulty and 100 is no difficulty at all (or best quality of life). Data from visits 2 through 5.

Interventions

  • OTHER Clinical evaluation
  • OTHER Performance based measures
  • OTHER Subjective measures of vision-related quality of life

Trial Details

FieldValue
Enrollment Target 161 participants
Start Date 2011-10
Est. Completion 2017-06
Phase NA
Wills Eye

59 total trials

What the finished NCT01476644 record still lists

NCT01476644 is an interventional study that assigns participants to a tested intervention. The registered 161 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 3 interventions - of which Clinical evaluation is the first listed.

NCT01476644 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01476644 about?

NCT01476644 is a clinical study titled "How Has Glaucoma Affected Your Quality of Life?". Hypothesis 1: Self-reported health-related quality of life decreases as vision impairment worsens in subjects with glaucoma. Hypothesis 2: Changes in health-related quality of life are associated with changes in clinical measures of vision and performance-based measures of visual function.

What is the current status of trial NCT01476644?

This trial is currently completed. It is a NA study. The enrollment target is 161 participants. The study started on 2011-10. Estimated completion is 2017-06.

What interventions are being tested in trial NCT01476644?

The interventions under investigation include: Clinical evaluation (OTHER), Performance based measures (OTHER), Subjective measures of vision-related quality of life (OTHER).

Who is sponsoring clinical trial NCT01476644?

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

How this trial's enrollment target compares

Where NCT01476644's enrollment target sits among peer trials

161 628th of 2000 higher than 1,373 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT06391034 · 161 participants · Phase 2

    Magnetic Resonance (MR) Imaging With Hyperpolarized 13C-Pyruvate +/- 13C,15N-Urea in Patients With Prostate Cancer

  • NCT06546670 · 161 participants · Phase 1

    A Phase I/II Study of ITU512 in Healthy Participants and Patients With Sickle Cell Disease

  • NCT06616766 · 161 participants · Phase 1

    A Phase 1/2, Open-label, Multicenter, FIH Study to Evaluate Safety, Tolerability, PK and Anti-tumor Activity of YH42946

  • NCT06752356 · 161 participants · Phase 3

    A Study Investigating Intravenous Human Normal Immune Globulin (IGIV) 10% in Subjects With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01476644, the US trial registry maintained by the National Library of Medicine. NCT01476644 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.