Goal directed fluid therapy guided by non invasive cardiometry in kasai procedure

Goal directed fluid therapy guided by non invasive cardiometry in kasai procedure: a randomized controlled trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

PACTR

Registry ID

PACTR202502715424419

Enrollment

Registered

2025-02-03

Start date

2025-01-01

Completion date

Unknown

Last updated

2026-01-27

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

Conditions

Anaesthesia

Interventions

control group

electrical cardiometry

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged 8 -12 weeks from both genders, American Society of Anesthesia (ASA) classification II, candidate for Kasai operation

Exclusion criteria

Exclusion criteria: • Patients with other congenital anomalies with known haemodynamic instability (e.g., ventricular septal defect, valvular lesions and arrhythmia). • Patients with uncontrolled renal dysfunction. • Preoperative haemodynamic instability. • Patient’s parent refusal to participate in the study.

Design outcomes

Primary

Measure	Time frame
To assess achieving the target of euvolumia and adequate tissue perfusion.	—

Secondary

Measure	Time frame
investigate the hemodynamic stability and record the postoperative complication and ICU stay.	—

Countries

Egypt

Contacts

Public Contacthanaa rashed

lecturer of anasthesia

hanaarashed2020@yahoo.com01001378542

Outcome results

None listed

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