# A Novel Mutation of the Spectrin Gene

> **NCT00723567** · — · COMPLETED · sponsor: **University of Utah** · enrollment: 12 (actual)

## Conditions studied

- Hereditary Elliptocytosis (HE)
- Hereditary Pyropoikilocytosis (HPP)

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00723567
- **Lead sponsor:** University of Utah
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2008-02
- **Primary completion:** 2008-12
- **Final completion:** 2008-12
- **Target enrollment:** 12 (ACTUAL)
- **Last updated:** 2009-02-19

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00723567

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00723567, "A Novel Mutation of the Spectrin Gene". Retrieved via AI Analytics 2026-06-05 from https://api.ai-analytics.org/clinical/NCT00723567. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*