Evaluation of the efficacy and safety of thromboprophylaxis regimens in patients after the Fontan procedure

Evaluation of the efficacy and safety of thromboprophylaxis regimens in patients after the Fontan procedure - Evaluation of the efficacy and safety of thromboprophylaxis regimens in patients after the Fontan procedure

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000044127

Enrollment

3000

Registered

2021-05-07

Start date

2021-04-07

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Patients after the Fontan procedure

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who underwent fontan procedure between June 2011 and September 2019 included in the data set from March 2011 to September 2020

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Onset of first thromboembolism for 1 year	—

Secondary

Measure	Time frame
Occurrence of bleeding events for 1 year	—

Countries

Japan

Contacts

Public ContactMasayuki Ohbayashi

Showa University Department of Pharmacotherapy, Department of Clinical Pharmacy,School of Pharmacy

ohbayashi@pharm.showa-u.ac.jp03-3784-8221

Outcome results