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NCT03866590: PIECE

Pyruvate Kinase Deficiency Epidemiological Study (PIECE)

Completed Last updated 9 February 2023
What this trial tests

trial in Pyruvate Kinase Deficiency in 75 participants. Completed in 31 May 2021.

Timeline
13 January 2020
Primary endpoint
31 May 2021
31 May 2021

Quick facts

Lead sponsorCENTOGENE GmbH Rostock
StatusCompleted
Study typeOBSERVATIONAL
Enrollment75
Start date13 January 2020
Primary completion31 May 2021
Estimated completion31 May 2021
Sites1 location across United States

Conditions studied

Sponsor

CENTOGENE GmbH Rostock

Who can join

Adults 5 to 30, any sex, with Pyruvate Kinase Deficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Pyruvate kinase deficiency (PKD) is the most common red cell glycolytic enzyme defect causing hereditary non-spherocytic hemolytic anemia, caused by mutations in the PKLR gene. The main goal of this study is the diagnosis of pyruvate kinase deficiency in patients who exhibit chronic anaemia and/or splenomegaly and/or judiance and/or hyperbilirubinemia and/or history of prolonged neonatal jaundice and/ or cholelithiasis of undetermined aetiology.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Pyruvate Kinase Deficiency

Currently open trials in the same condition.

Other CENTOGENE GmbH Rostock trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03866590.

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