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NCT00723567 · ClinicalTrials.gov registry record
A Novel Mutation of the Spectrin Gene
A clinical trial, sponsored by University of Utah.
- Completed
- Registry status
- 12
- Enrollment target
NCT00723567 is a clinical trial that has completed, run by University of Utah. The registered enrollment target is 12 participants.
The verdict
NCT00723567 has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- 12 participants
- Enrollment target
Study Summary
The purpose of this study is to find a gene or its mutation (an altered gene) that puts individuals at risk for developing HE or HPP.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2008-02 |
| Est. Completion | 2008-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00723567
The ClinicalTrials.gov registry entry for NCT00723567 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT00723567 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00723567 about?
NCT00723567 is a clinical study titled "A Novel Mutation of the Spectrin Gene". The purpose of this study is to find a gene or its mutation (an altered gene) that puts individuals at risk for developing HE or HPP.
What is the current status of trial NCT00723567?
This trial is currently completed. The enrollment target is 12 participants. The study started on 2008-02. Estimated completion is 2008-12.
Who is sponsoring clinical trial NCT00723567?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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