Review of French Cases of Glutathione Synthetase Deficiency

• Conditions: The Glutathione Synthetase Deficiency

• Registration Number: NCT02830867
• Lead Sponsor: University Hospital, Strasbourg, France

Brief Summary

The glutathione synthetase deficiency, inborn error of metabolism of autosomal recessive inheritance, is a rare disease (70 patients described in the world). The outcome of these patients and potential complications of this disease are not, to date, yet all known and described.

Detailed Description

Not available

Study Timeline

• Status Verified: 2016-01
• Study First Submitted: 2016-06-17
• Study Start: 2016-07
• Study First Submitted QC: 2016-07-08
• Study First Posted: 2016-07-13
• Last Update Submitted: 2018-01-08
• Last Update Posted: 2018-01-10
• Primary Completion: 2018-10
• Study Completion: 2018-10

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Immunologically determining human acid glutathione S-transferase in a human assay sample	1 hour after hospitalization

Trial Locations

Locations (1)

Service D'Urgences Medicales Pediatriques; 🇫🇷 Strasbourg, France