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NCT02995538 · ClinicalTrials.gov registry record

Neurogenetics Patient Registry

A clinical trial of Neurogenetic Disorders, sponsored by University of Pittsburgh.

Recruiting
Registry status
1,000
Enrollment target
1
Study location

NCT02995538: Recruiting study of Neurogenetic Disorders, sponsored by University of Pittsburgh.

NCT02995538 is a study of Neurogenetic Disorders that is actively recruiting participants, run by University of Pittsburgh. The registered enrollment target is 1,000 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02995538, a study of Neurogenetic Disorders, is actively recruiting participants, sponsored by University of Pittsburgh.

RECRUITING
Registry status
1,000 participants
Enrollment target
1
Study location

Study Summary

The objective of this project is to develop a Neurogenetics patient database and bio repository - which includes clinical information regarding history, physical examination, laboratory testing including genetic testing (NextGen sequencing including whole exome and whole genome sequencing, SNParray, etc.), neuroradiology studies, neurophysiology studies - all ordered as clinically deemed appropriate, natural history from clinical longitudinal follow-up and to use de-identified information from this registry/ repository, when appropriate for clinical and translational research.

Primary Outcome

Next generation sequencing, if clinically appropriate will be ordered through available commercial labs as approved by the patient's insurance company. If insurance coverage is denied research testing will be ordered after informed consent and pretesting counseling, to be done through our collaborative labs.

Conditions Studied

Study Locations (1)

Pennsylvania

  • Children's Hospital of Pittsburgh of UPMC - Pittsburgh

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2017-01-30
Est. Completion 2028-01
University of Pittsburgh

1,238 total trials

What NCT02995538 shows while recruiting

NCT02995538 is an observational study that tracks outcomes without assigning an intervention. Its 1,000 participants enrollment target places it among the larger protocols in the corpus.

The record links to 1 condition, with Neurogenetic Disorders appearing as the primary indexed condition, and to 0 interventions.

NCT02995538 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02995538 about?

NCT02995538 is a clinical study titled "Neurogenetics Patient Registry". The objective of this project is to develop a Neurogenetics patient database and bio repository - which includes clinical information regarding history, physical examination, laboratory testing including genetic testing (NextGen sequencing including whole exome and whole genome sequencing, SNParray,...

What is the current status of trial NCT02995538?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2017-01-30. Estimated completion is 2028-01.

What conditions does trial NCT02995538 study?

This clinical trial studies the following conditions: Neurogenetic Disorders.

Who is sponsoring clinical trial NCT02995538?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02995538 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT02995538, the US trial registry maintained by the National Library of Medicine. NCT02995538 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.