Population pharmacokinetics of digoxin in Chinese neonates and infants: a records based retrospective cohort study

Population pharmacokinetics of digoxin in Chinese neonates and infants

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-RCH-13003435

Enrollment

Unknown

Registered

2013-08-09

Start date

2010-01-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Congestive heart failure, rapid atrial fibrillation, atrial flutter

Interventions

2 :blood samplling

Eligibility

Sex/Gender

All

Age

No minimum to 1 Years

Inclusion criteria

Inclusion criteria: Hospitalized patients (aged 0 to 1) who orally administered digoxin elixir more than 6 days and drawn the blood over 6 hours from the drug administration were included in this study.

Exclusion criteria

Exclusion criteria: Patients, whose data are not complete (especially the ones with blood sampling time missing), or suffered serious hepatic and renal dysfunction were excluded from the study.

Design outcomes

Primary

Measure	Time frame
drug concentration;	—

Countries

China

Contacts

Public ContactZhiping Li

zplifudan@gmail.com+86 13816880750

Outcome results

None listed

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