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Method verification of Biotinidase estimation

Analytical verification of a biotinidase activity assay: Assessment of linearity, precision, accuracy. - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/085099
Enrollment
20
Registered
2025-04-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Control Intervention1: NIL: NIL

Sponsors

Pooja Bandiwaddar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Any left over samples after the assays. No clot seen in blood. Samples collected with proper procedure.

Exclusion criteria

Exclusion criteria: Hemolysed Sample. Icteric samples

Design outcomes

Primary

MeasureTime frame
To verify the accuracy and reliability of the biotinidase enzyme activity assay in serum for the detection of biotinidase deficiency.Timepoint: 12 Weeks—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactPooja Bandiwaddar

KLEs Jawaharlal Nehru Medical College Belagavi

dranura9@gmail.com9481738133

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026