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Effectiveness of preoperative use of noninvasive ventilation (NIV) in patients with living donor liver transplantation

Effectiveness of preoperative use of noninvasive ventilation (NIV) in patients with living donor liver transplantation - Preoperative use of noninvasive ventilation for living donor liver transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008986
Enrollment
40
Registered
2012-09-27
Start date
2012-10-01
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

Living donor liver transplantation

Interventions

The patients receive NIV for 2 to 3 hours in the daytime. Pressure support is increased until the maximal level tolerated by the patients is reached. The patients continue the current treatments.

Sponsors

Department of respiratory management and sleep control medicine, Graduate School of Medicine, Kyoto University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Recipients of living donor liver transplantation. 2. Analysis of arterial blood gas reveals PaO2 as less than 60 mmHg or PaCO2 as more than 7.3 or analysis of nocturnal monitoring reveals PtCO2 more than 45 mmHg or SpO2 less than 90%.

Exclusion criteria

Exclusion criteria: 1. recipients of emergency living donor liver transplantation 2. recipients of living donor liver retransplantation 3. Patients need to receive oxygen therapy or NIV therapy by analysis of arterial blood gas and nocturnal monitoring. 4. unstable asthma or mild chronic obstructive pulmonary disease (percent predicted FEV1) 5. pneumothorax within 6 months 6. patients complicated with chronic lung disease 7. patients complicated with acute infections. 8. patients received NIV

Design outcomes

Primary

MeasureTime frame
1. arterial blood oxygen level 2. alveolar-arterial difference in partial pressure of oxygen

Secondary

MeasureTime frame
1. lung function testing (forced expiratory volume in one second (FEV1), FEV1/forced vital capacity, maximum mid-expiratory flow rate, respiratory muscle force) 2. preoperative chest X ray 3. postoperative arterial blood gas 4. postoperative pulmonary infection 5. postoperative death

Countries

Japan

Contacts

Public ContactSatoshi Hamada

Graduate School of Medicine, Kyoto University Department of Respiratory Medicine

sh1124@kuhp.kyoto-u.ac.jp075-751-3830

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026