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

RECRUITING

Studying Health Outcomes After Treatment in Patients With Retinoblastoma

NCT03932786 · View on ClinicalTrials.gov ↗

Study Summary

This trial studies health outcomes after treatment in patients with retinoblastoma. Gathering health information over time from patients and family members through vision assessments, samples of tissue and saliva, and questionnaires may help doctors learn more about what causes retinoblastoma, identify long-term health outcomes for patients with retinoblastoma, and find out which therapies may be the best for treating retinoblastoma

Interventions

  • OTHER Laboratory Biomarker Analysis
  • PROCEDURE Biospecimen collection
  • OTHER Questionnaire administration
  • OTHER Quality of life assessment
  • OTHER Vision assessment

Study Locations (11)

Illinois

  • Lurie Children's Hospital — Chicago
  • University of Illinois, Chicago — Chicago

Texas

  • MD Anderson Cancer Center — Houston
  • Texas Childeren's Hospital — Houston

Minnesota

  • University of Minnesoa — Minneapolis

Missouri

  • Washington School of Medicine at St. Louis — St Louis

Ohio

  • Cincinnati Children's Hospital Medical Center — Cincinnati

Pennsylvania

  • Children's Hospital of Philadelphia — Philadelphia

Tennessee

  • Vanderbilt-Ingram Cancer Center — Nashville

Wisconsin

  • Children's Hospital of Wisconsin — Milwaukee

Trial Details

FieldValue
Enrollment Target 900 participants
Start Date 2019-01-24
Est. Completion 2031-01

Sponsor

Vanderbilt-Ingram Cancer Center

143 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03932786

The ClinicalTrials.gov registry entry for NCT03932786 describes a study currently listed as recruiting. 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 900 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt-Ingram Cancer Center, which has 143 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Cancer Survivor appearing as the primary indexed condition, and to 5 interventions — of which Laboratory Biomarker Analysis 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: NCT03932786 reports 11 study locations spanning 9 distinct geographic areas — top geographies include Illinois, Texas, 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 NCT03932786 about?

NCT03932786 is a clinical study titled "Studying Health Outcomes After Treatment in Patients With Retinoblastoma". This trial studies health outcomes after treatment in patients with retinoblastoma. Gathering health information over time from patients and family members through vision assessments, samples of tissue and saliva, and questionnaires may help doctors learn more about what causes retinoblastoma, ident...

What is the current status of trial NCT03932786?

This trial is currently recruiting. The enrollment target is 900 participants. The study started on 2019-01-24. Estimated completion is 2031-01.

What conditions does trial NCT03932786 study?

This clinical trial studies the following conditions: Cancer Survivor, Retinoblastoma, Unilateral Retinoblastoma, Intraocular Retinoblastoma, Biological Sibling. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03932786?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Biospecimen collection (PROCEDURE), Questionnaire administration (OTHER), Quality of life assessment (OTHER), Vision assessment (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03932786?

This trial is sponsored by Vanderbilt-Ingram Cancer Center, which has 143 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03932786 being conducted?

This trial has 11 study locations across Illinois, Minnesota, Missouri, Ohio, Pennsylvania. 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