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COMPLETED

Patient Reported Outcomes With LASIK: PROWL-2

NCT01655420 · View on ClinicalTrials.gov ↗

Study Summary

This study evaluates a questionaire designed to measure satisfaction and ophthalmic-related quality of life (QoL) of 300 civilian participants prior to and three months following state-of-the-art laser in situ keratomileusis (LASIK).

Interventions

  • PROCEDURE LASIK

Study Locations (5)

California

  • Stanford University School of Medicine — Stanford

Indiana

  • 20/20 Institute — Indianapolis

Kansas

  • Durrie Vision — Overland Park

Maryland

  • Johns Hopkins University School of Medicine — Baltimore

South Dakota

  • Vance Thompson Vision — Sioux Falls

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2012-07

Sponsor

Food and Drug Administration (FDA)

35 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01655420

The ClinicalTrials.gov registry entry for NCT01655420 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Food and Drug Administration (FDA), which has 35 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Laser in Situ Keratomileusis appearing as the primary indexed condition, and to 1 intervention — of which LASIK is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01655420 reports 5 study locations spanning 5 distinct geographic areas — top geographies include California, Indiana, Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01655420 about?

NCT01655420 is a clinical study titled "Patient Reported Outcomes With LASIK: PROWL-2". This study evaluates a questionaire designed to measure satisfaction and ophthalmic-related quality of life (QoL) of 300 civilian participants prior to and three months following state-of-the-art laser in situ keratomileusis (LASIK).

What is the current status of trial NCT01655420?

This trial is currently completed. The enrollment target is 300 participants. The study started on 2012-07.

What conditions does trial NCT01655420 study?

This clinical trial studies the following conditions: Laser in Situ Keratomileusis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01655420?

The interventions under investigation include: LASIK (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01655420?

This trial is sponsored by Food and Drug Administration (FDA), which has 35 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01655420 being conducted?

This trial has 5 study locations across California, Indiana, Kansas, Maryland, South Dakota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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