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Incentive Spirometer in Liver Transplant Recipients

Effect of Incentive Spirometer on Arterial Blood Gases in Liver Transplant Recipients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07318766
Acronym
LT
Enrollment
40
Registered
2026-01-06
Start date
2024-11-01
Completion date
2025-11-01
Last updated
2026-01-06

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

Conditions

Liver Transplant Disorder

Keywords

Liver Transplant, Incentive Spirometer, Arterial Blood Gas

Brief summary

This study evaluated the effect of adjunctive incentive spirometer on arterial blood gases (ABGs) and early postoperative recovery in liver transplant recipients.

Detailed description

In this prospective , randomized study, 40 adults undergoing living-donor liver transplantation (LT) were assigned to standard post-transplant mobilization and breathing exercises alone (n=20) or standard exercises plus structured IS training (n=20). Arterial blood gases ABG parameters (pH, PO₂, PCO₂, HCO₃-, SpO₂) were measured at baseline and on postoperative days 1-3. Linear mixed-effects models assessed group differences in ABG trajectories; slope analyses quantified decline and recovery phases. Secondary outcomes included intensive care unit (ICU) and hospital length of stay (LOS) and Post-operative pulmonary complications incidence.

Interventions

DEVICEIncentive Spirometry

An intensive spirometry (IS) is a device that measures inhaled air volume and provides visual feedback as a piston rises during inspiration. It is widely used in respiratory and physical therapy to encourage slow, deep breathing, which helps expand the lungs, open airways, and mimic the natural deep breaths seen in yawning or sighing.

Sponsors

El-Sahel Teaching Hospital
CollaboratorOTHER_GOV
National Hepatology & Tropical Medicine Research Institute
CollaboratorOTHER_GOV
Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

open label, parallel, prospective, randomized study

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. age between 18 and 65 years, 2. scheduled to undergo Living Donor Liver Transplant (LDLT) as recipients 3. able to understand and follow instructions for incentive spirometry use

Exclusion criteria

1. multiorgan transplantation 2. moderate-to-severe pleural effusion at baseline 3. persistent elevation in renal function tests 4. history of bleeding esophageal varices within the preceding month 5. multicentric hepatocellular carcinoma (HCC) 6. active smoking 7. decompensated cardiac disease 8. alcoholic hepatitis as the primary etiology 9. cognitive impairment or blindness precluding participation in the rehabilitation protocol.

Design outcomes

Primary

MeasureTime frameDescription
Arterial blood gas (ABG) parameters3 days (assessed at four time points: baseline (within 48 hours before surgery) and on post-operative days 1, 2, and 3)Arterial pH
Arterial Blood Gas (ABG) parameters3 days (assessed at four time points: baseline (within 48 hours before surgery) and at day 1,2, and 3 post-surgery)(2) partial pressure of carbon dioxide (PCO2, mmHg)
Arterial Blood Gas (ABG) Parameters3 days (assessed at four time points: baseline (within 48 hours before surgery) and at day 1, 2, and 3 post-surgery)(4) bicarbonate concentration (HCO3-, mEq/L)

Secondary

MeasureTime frameDescription
length of intensive care unit (ICU) stayPerioperative period (Hospital stay duration)The length of intensive care unit (ICU) stay (days)
hospital stayPerioperative period (Hospital Stay duration)total length of hospital stay (days)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026