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COMPLETED NA

A Pilot Clinical Trial of Overminus Spectacle Therapy for Intermittent Exotropia

NCT02223650 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this short-term, pilot randomized trial comparing 2.50 diopters (D) overminus lens treatment vs. non-overminus (spectacles without overminus or no spectacles) in children with intermittent exotropia (IXT) 3 to \<7 years of age is to determine whether to proceed to a full-scale, longer-term randomized trial.

Conditions Studied

Interventions

  • DEVICE Overminus treatment
  • DEVICE Non-overminus treatment

Study Locations (2)

California

  • Marshall B. Ketchum University — Fullerton

Minnesota

  • Mayo Clinic — Rochester

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2014-12
Est. Completion 2015-07
Phase NA

Sponsor

Jaeb Center for Health Research

134 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02223650

The ClinicalTrials.gov registry entry for NCT02223650 describes a study currently listed as completed. It is categorized as NA, 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 58 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Jaeb Center for Health Research, which has 134 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 Intermittent Exotropia appearing as the primary indexed condition, and to 2 interventions — of which Overminus treatment 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: NCT02223650 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Minnesota. 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 NCT02223650 about?

NCT02223650 is a clinical study titled "A Pilot Clinical Trial of Overminus Spectacle Therapy for Intermittent Exotropia". The objective of this short-term, pilot randomized trial comparing 2.50 diopters (D) overminus lens treatment vs. non-overminus (spectacles without overminus or no spectacles) in children with intermittent exotropia (IXT) 3 to \<7 years of age is to determine whether to proceed to a full-scale, long...

What is the current status of trial NCT02223650?

This trial is currently completed. It is a NA study. The enrollment target is 58 participants. The study started on 2014-12. Estimated completion is 2015-07.

What conditions does trial NCT02223650 study?

This clinical trial studies the following conditions: Intermittent Exotropia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02223650?

The interventions under investigation include: Overminus treatment (DEVICE), Non-overminus treatment (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02223650?

This trial is sponsored by Jaeb Center for Health Research, which has 134 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02223650 being conducted?

This trial has 2 study locations across California, Minnesota. 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