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Natural History Study of Pyruvate Dehydrogenase Deficiency | Clinical Trials | Clareo Health

UNKNOWNNCT05257005

Natural History Study of Pyruvate Dehydrogenase Deficiency

Pyruvate dehydrogenase (PDH) deficiency is one of the most common mitochondrial disorders. Patients with this genetic condition have difficulty utilising carbohydrates to produce energy and develop a ...

Lead sponsor: Great Ormond Street Hospital for Children NHS Foundation Trust•1 locations•View source on ClinicalTrials.gov

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Contacts

Nandaki Keshavan, MA, MB BChir

CONTACT

020 7905 2608 n.keshavan@ucl.ac.uk

Vanshree Patel, PhD

CONTACT

0207 905 42271 vanshree.patel@gosh.nhs.uk

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Trial of Dichloroacetate in Pyruvate Dehydrogenase Complex Deficiency:

NCT02616484 · Pyruvate Dehydrogenase Complex Deficiency

Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: December 5, 2023Terms

Trial snapshot

StatusUNKNOWN

Phase—

Enrollment50

Start dateNov 2020

Last updatedDec 5, 2023

Condition

Pyruvate Dehydrogenase Complex Deficiency Pyruvate Dehydrogenase E1 Alpha Deficiency Pyruvate Dehydrogenase E1-Beta Deficiency Pyruvate Dehydrogenase E2 Deficiency Pyruvate Dehydrogenase Phosphatase Deficiency

Locations shown

Great Ormond Street Hospital

London

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: December 5, 2023Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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