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COMPLETED

Pyruvate Kinase Deficiency Natural History Study

NCT02053480 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to describe the range and incidence of symptoms, treatments, and complications related to pyruvate kinase deficiency (PKD). Eligible patients are those of all ages with known PKD or with a hemolytic anemia and a family member with PKD. The study will collect retrospective medical history, routine clinical care data, and quality of life measures at baseline and annually for patients with PKD.

Study Locations (20)

Massachusetts

  • Boston Children's Hospital — Boston
  • University of Massachusetts Medical Center — Worcester

Ohio

  • Nationwide Children's Hospital — Columbus
  • DDC Clinic for Special Needs Children — Middlefield

Pennsylvania

  • Children's Hospital of Philadelphia — Philadelphia
  • Central Pennsylvania Clinic — Strasburg

Arizona

  • Phoenix Children's Hospital — Phoenix

California

  • Stanford University — Palo Alto

Georgia

  • Children's Hospital of Atlanta — Atlanta

Illinois

  • Lurie Children's Hospital — Chicago

Michigan

  • Wayne State University School of Medicine — Detroit

Trial Details

FieldValue
Enrollment Target 254 participants
Start Date 2013-12
Est. Completion 2020-05

Sponsor

Boston Children's Hospital

752 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02053480

The ClinicalTrials.gov registry entry for NCT02053480 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 254 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Children's Hospital, which has 752 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Pyruvate Kinase Deficiency appearing as the primary indexed condition, and to 0 interventions. 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: NCT02053480 reports 20 study locations spanning 17 distinct geographic areas — top geographies include Massachusetts, Ohio, Pennsylvania. 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 NCT02053480 about?

NCT02053480 is a clinical study titled "Pyruvate Kinase Deficiency Natural History Study". The purpose of this study is to describe the range and incidence of symptoms, treatments, and complications related to pyruvate kinase deficiency (PKD). Eligible patients are those of all ages with known PKD or with a hemolytic anemia and a family member with PKD. The study will collect retrospectiv...

What is the current status of trial NCT02053480?

This trial is currently completed. The enrollment target is 254 participants. The study started on 2013-12. Estimated completion is 2020-05.

What conditions does trial NCT02053480 study?

This clinical trial studies the following conditions: Pyruvate Kinase Deficiency, Congenital Non-Spherocytic Hemolytic Anemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT02053480?

This trial is sponsored by Boston Children's Hospital, which has 752 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02053480 being conducted?

This trial has 20 study locations across Arizona, California, Georgia, Illinois, Massachusetts. 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