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Genetic Load and Phenotype in Aggressive AMD

NCT01650948 · View on ClinicalTrials.gov ↗

Study Summary

Patients with AMD will provide cheek cell samples to determine if their is a correlation between genotype (DNA markers) and phenotype (the type of AMD the patient has).

Interventions

  • DEVICE RetnaGene AMD LDT

Study Locations (3)

California

  • Pacific Eye Associates — San Francisco

Kentucky

  • Retina Associates of Kentucky — Lexington

Tennessee

  • Tennessee Retina — Nashville

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2012-07
Est. Completion 2013-12

Sponsor

Sequenom

43 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01650948

The ClinicalTrials.gov registry entry for NCT01650948 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 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sequenom, which has 43 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 Age-related Macular Degeneration appearing as the primary indexed condition, and to 1 intervention — of which RetnaGene AMD LDT 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: NCT01650948 reports 3 study locations spanning 3 distinct geographic areas — top geographies include California, Kentucky, Tennessee. 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 NCT01650948 about?

NCT01650948 is a clinical study titled "Genetic Load and Phenotype in Aggressive AMD". Patients with AMD will provide cheek cell samples to determine if their is a correlation between genotype (DNA markers) and phenotype (the type of AMD the patient has).

What is the current status of trial NCT01650948?

This trial is currently completed. The enrollment target is 100 participants. The study started on 2012-07. Estimated completion is 2013-12.

What conditions does trial NCT01650948 study?

This clinical trial studies the following conditions: Age-related Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01650948?

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

Who is sponsoring clinical trial NCT01650948?

This trial is sponsored by Sequenom, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01650948 being conducted?

This trial has 3 study locations across California, Kentucky, Tennessee. 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