# Hereditary Paraganglioma: Evaluation of Screening Methods to Detect Tumors in SDH Positive Carriers

> **NCT00188019** · NA · COMPLETED · sponsor: **University Hospital, Angers** · enrollment: 248 (actual)

## Conditions studied

- Paraganglioma
- Pheochromocytoma

## Interventions

- **PROCEDURE:** diagnosis methods

## Key facts

- **NCT ID:** NCT00188019
- **Lead sponsor:** University Hospital, Angers
- **Sponsor class:** OTHER_GOV
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2005-11
- **Primary completion:** 2013-11
- **Final completion:** 2013-11
- **Target enrollment:** 248 (ACTUAL)
- **Last updated:** 2015-07-23

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00188019

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00188019, "Hereditary Paraganglioma: Evaluation of Screening Methods to Detect Tumors in SDH Positive Carriers". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT00188019. Licensed CC0.

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