CompletedNot applicableNCT00188019
Hereditary Paraganglioma: Evaluation of Screening Methods to Detect Tumors in SDH Positive Carriers
Studying Hereditary pheochromocytoma-paraganglioma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospital, Angers
- Principal Investigator
- Vincent Rohmer, MDUniversity Angers Hospital
- Intervention
- diagnosis methods(procedure)
- Enrollment
- 248 target
- Eligibility
- 6 years · All sexes
- Timeline
- 2005 – 2013
Study locations (1)
- Européen Georges Pompidou Hospital, Paris, France
Collaborators
Assistance Publique - Hôpitaux de Paris
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT00188019 on ClinicalTrials.govOther trials for Hereditary pheochromocytoma-paraganglioma
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