End-Stage Liver DiseaseNCT07414095
Multidimensional Frailty Assessment and Post-Transplant Outcomes in Liver Transplant Candidates
An observational study of End-Stage Liver Disease and Liver Transplantation, run by Izmir Bakircay University at 1 site in Turkey (Türkiye).
Trial summary
This study will evaluate frailty, nutrition, sarcopenia, and psychological health in people waiting for a liver transplant. The purpose is to understand how these factors affect outcomes before and after transplantation. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- End-Stage Liver Disease, Liver Transplantation, Cirrhosis
- What is being tested?
- Comprehensive Observational Assessment in Liver Transplant Candidates
- How many people
- 60 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 15 Dec 2025to Aug 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: The study population consists of patients listed as liver transplant candidates at a private hospital in Izmir, Turkey.
Who may be able to join
- Being listed as a liver transplant candidate
- Age between 18 and 65 years
- Ability to understand the Turkish language
Who cannot join
- Presence of orthopedic and/or neurological problems severe enough to prevent completion of assessment tools
- Inability to understand verbal commands
- Being a recipient of multiple organ transplants
- Presence of serious active extrahepatic malignancy
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Turkey (Türkiye)1 site, 1 recruiting
- Recruiting
Izmir University of Economics Medical Point Hospital
Izmir
About this study
Official title: Investigation of the Relationship Between Frailty, Sarcopenia, Malnutrition, and Psychosocial Parameters and Post-Transplant Outcomes in Liver Transplant Candidates
This study will evaluate frailty, nutrition, sarcopenia, and psychological health in people waiting for a liver transplant. The purpose is to understand how these factors affect outcomes before and after transplantation. By identifying patients at higher risk early, the study aims to support the development of better care programs in the future.
Participants will complete simple tests of physical strength, walking speed, and daily activity levels. Their nutrition and psychological well-being will also be assessed. The study will then look at how these results relate to medical scores used in liver disease and to outcomes after transplant, such as hospital stay, complications, or survival.
Adults aged 18-65 years who are on the liver transplant waiting list and can understand Turkish are eligible to join.
- Conditions
- End-Stage Liver Disease, Liver Transplantation, Cirrhosis
- Being tested
- Comprehensive Observational Assessment in Liver Transplant Candidates
- Keywords
- Liver Transplant Candidates, Frailty, Sarcopenia, Malnutrition, Psychosocial Health
- Medical subject headings
- End Stage Liver Disease, Fibrosis, Frailty, Sarcopenia, Malnutrition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Comprehensive Observational Assessment in Liver Transplant CandidatesOther
This study involves a comprehensive, multidimensional assessment of liver transplant candidates focusing on frailty, sarcopenia, malnutrition, and psychosocial status. Frailty will be measured using the Liver Frailty Index (LFI), 6-Minute Walk Test (6MWT), Karnofsky Performance Status (KPS), and Activities of Daily Living (ADL). Sarcopenia will be evaluated through handgrip strength, Appendicular Skeletal Muscle Mass (ASM)/Skeletal Muscle Index (SMI), and 4-meter gait speed. Malnutrition will be assessed using the Nutritional Risk Index (NRI) and phase angle derived from bioelectrical impedance analysis. Psychosocial status will be measured with the Hospital Anxiety and Depression Scale (HADS). Clinical parameters (MELD-Na, Child-Pugh, CKI-OKN) will be recorded. Post-transplant adverse outcomes including prolonged hospital and ICU stay, postoperative complications, early mortality, and duration of mechanical ventilation will be monitored up to 30 days after surgery.
| Study group | Role | What they receive |
|---|---|---|
| Adult Liver Transplant Candidates | This cohort includes adult patients (aged 18-65 years) who are on the liver transplant waiting list and able to understand Turkish. Participants will undergo assessments of frailty, sarcopenia, malnutrition, and psychosocial health. No therapeutic intervention will be applied; this is an observational study. Clinical outcomes after transplantation, such as length of ICU stay, hospital discharge time, complications, and survival, will be recorded prospectively. Receives: Other: Comprehensive Observational Assessment in Liver Transplant Candidates |
What is being measured
The primary outcome is the main question the study is designed to answer.
Liver Frailty Index (LFI)
Frailty will be assessed using the Liver Frailty Index (LFI), which is calculated from three standardized physical performance tests: grip strength (kg, average of three trials), chair stands (seconds to complete five repetitions), and balance test (seconds, up to 10 seconds in three positions). LFI score will be calculated according to the standard LFI formula. Frailty severity will be categorized as:
≥4.5: Severe frailty 3.2-4.4: Moderate frailty <3.2: Not frail Unit of Measure: LFI score (continuous) Direction: Higher scores indicate greater frailty (worse outcome).
Measured: At hospital admission when liver transplantation is confirmed.
6-Minute Walk Test (6MWT) Distance
The 6-minute walk test (6MWT) will be conducted according to European Respiratory Society and American Thoracic Society guidelines along a 30-meter corridor. Participants will be instructed to walk as far as possible in six minutes. Distance walked will be recorded in meters and rounded to the nearest meter. Oxygen saturation, heart rate, blood pressure, and fatigue (Modified Borg Scale) will be recorded before and after the test, with continuous SpO₂ and heart rate monitoring during the walk. Frailty classification will be based on the following thresholds: <250 m (severe frailty), 250-350 m (moderate frailty), >350 m (not frail).
Unit of Measure: Meters (continuous) Direction: Higher walking distance indicates lower frailty (better outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Karnofsky Performance Status (KPS)
The Karnofsky Performance Status (KPS) is a subjective measure of frailty, originally developed for oncology and subsequently applied in cirrhosis. The scale ranges from 0% (death) to 100% (normal; no complaints; no evidence of disease), scored in 10-point increments. Applicable to both hospitalized and ambulatory patients. Frailty classification will be based on the following thresholds:
0-40% = Severe frailty 50-70% = Moderate frailty
≥80% = Not frail Unit of Measure: Percentage (%) Direction: Higher KPS score indicates lower frailty (better outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Activities of Daily Living (ADL)
The Activities of Daily Living (ADL) scale is a subjective measure of frailty, developed to assess functional status in aging populations. It evaluates six functions: bathing, dressing, toileting, continence, transferring, and feeding. The scale is self-reported and scored from 0 (dependent) to 6 (independent). Frailty classification will be based on the following thresholds: ≥2 difficulties (severe frailty), 1 difficulty (moderate frailty), and 0 difficulties (not frail).
Unit of Measure: Score (0-6) Direction: Higher scores indicate lower frailty (better outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Secondary outcomes (15)
Nutritional Risk Index (NRI)
Nutritional status will be assessed using the Nutritional Risk Index (NRI). The NRI score will be calculated using serum albumin level (g/dL), current body weight (kg), and usual body weight (kg) according to the following formula:
NRI = (15.19 × serum albumin [g/dL]) + (41.7 × current weight / usual weight)
Nutritional status will be categorized as follows:
NRI ≥ 100: No malnutrition 97.5 ≤ NRI < 100: Mild malnutrition 83.5 ≤ NRI < 97.5: Moderate malnutrition NRI < 83.5: Severe malnutrition Unit of Measure: NRI score Direction: Higher NRI values indicate better nutritional status.
Measured: At hospital admission when liver transplantation is confirmed.
Phase Angle Measured by Bioelectrical Impedance Analysis (BIA)
Phase angle will be measured using bioelectrical impedance analysis (BIA) as an indicator of cellular integrity and nutritional status. Measurements will be performed according to standard BIA procedures at the time of hospital admission.
Phase angle values will be categorized according to predefined study criteria as follows:
<4.4 degrees: Abnormal 4.4-5.4 degrees: Borderline
≥5.4 degrees: Normal Unit of Measure: Degrees Direction: Higher phase angle values indicate better cellular health and nutritional status.
Measured: At hospital admission when liver transplantation is confirmed.
Sarcopenia Diagnosis According to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) Criteria
Sarcopenia will be assessed according to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) criteria. Evaluation will include assessment of muscle strength, muscle mass, and physical performance using standardized measurement procedures at hospital admission.
Sarcopenia will be classified as:
Probable sarcopenia: Low muscle strength Sarcopenia: Low muscle strength and low muscle mass Severe sarcopenia: Low muscle strength, low muscle mass, and low physical performance Unit of Measure: Categorical classification (probable sarcopenia, sarcopenia, severe sarcopenia) Direction: Lower sarcopenia severity indicates better muscle status.
Measured: At hospital admission when liver transplantation is confirmed.
Handgrip Strength (HGS)
Handgrip strength will be measured using a hand dynamometer in the dominant hand following a standardized protocol (patient seated, elbow at 90 degrees, three trials, best value recorded). Low muscle strength will be defined according to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) criteria as <27 kg for men and <16 kg for women.
Unit of Measure: Kilograms (kg) Direction: Higher handgrip strength indicates better muscle strength and physical status.
Measured: At hospital admission when liver transplantation is confirmed.
Skeletal Muscle Index (SMI)
Skeletal Muscle Index (SMI) will be assessed using bioelectrical impedance analysis (BIA). Appendicular skeletal muscle mass (ASM) will be calculated as the sum of muscle mass of the upper and lower extremities. SMI will be derived by dividing ASM (kg) by height squared (m²), according to the formula:
SMI = ASM / height² Low muscle mass will be defined according to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) criteria as SMI <7.0 kg/m² for men and <5.5 kg/m² for women.
Unit of Measure: kg/m² Direction: Higher SMI values indicate better skeletal muscle mass and physical status.
Measured: At hospital admission when liver transplantation is confirmed.
Gait Speed (4-meter walk test)
Gait speed will be measured using the 4-meter walk test. Participants will be instructed to walk at their usual pace over a 4-meter course, and time will be recorded with a stopwatch. Gait speed will be calculated as distance (4 m) divided by time (seconds) and expressed in m/s. Low physical performance will be defined according to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) criteria as gait speed ≤0.8 m/s.
Unit of Measure: Meters per second (m/s) Direction: Higher gait speed indicates better physical performance.
Measured: At hospital admission when liver transplantation is confirmed.
Hospital Anxiety and Depression Scale - Anxiety Subscale (HADS-A)
Anxiety symptoms will be assessed using the anxiety subscale of the Hospital Anxiety and Depression Scale (HADS-A), which consists of 7 items. Each item is scored from 0 to 3, producing a total score ranging from 0 to 21. Higher scores indicate greater anxiety symptoms. A score of ≥10 will be considered indicative of clinically significant anxiety, based on the validated Turkish version of the scale.
Unit of Measure: HADS-A score (0-21) Direction: Higher scores indicate higher anxiety symptoms (worse outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Hospital Anxiety and Depression Scale - Depression Subscale (HADS-D)
Depressive symptoms will be assessed using the depression subscale of the Hospital Anxiety and Depression Scale (HADS-D), which consists of 7 items. Each item is scored from 0 to 3, producing a total score ranging from 0 to 21. Higher scores indicate greater depressive symptoms. A score of ≥7 will be considered indicative of clinically significant depression, based on the validated Turkish version of the scale.
Unit of Measure: HADS-D score (0-21) Direction: Higher scores indicate higher depressive symptoms (worse outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Hospital Anxiety and Depression Scale - Total Score (HADS Total)
Psychological distress will be assessed using the Hospital Anxiety and Depression Scale (HADS), a 14-item self-report questionnaire. Each item is scored from 0 to 3, producing a total score ranging from 0 to 42. The total score is calculated as the sum of all items (HADS Total = HADS-A + HADS-D). No validated universal cut-off exists for the total score; therefore, it will be analyzed as a continuous variable.
Unit of Measure: Total HADS score (0-42) Direction: Higher scores indicate greater psychological distress (worse outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Charlson Comorbidity Index - Orthotopic Liver Transplant (CCI-OLT)
Comorbidity burden will be assessed using the Charlson Comorbidity Index modified for orthotopic liver transplant candidates (CCI-OLT). The index includes five comorbidities with the following weights: COPD (3 points), coronary artery disease (2 points), connective tissue disease (2 points), renal insufficiency (2 points), and diabetes mellitus (1 point). Renal insufficiency is defined as serum creatinine >1.5 mg/dL in the most recent preoperative test. The total CCI-OLT score will be calculated as the sum of the weighted comorbidities.
Unit of Measure: CCI-OLT score (continuous) Direction: Higher scores indicate greater comorbidity burden (worse outcome).
Measured: At hospital admission when liver transplantation is confirmed.
Intensive Care Unit (ICU) Length of Stay
Length of stay in the intensive care unit (ICU) after orthotopic liver transplantation will be recorded. ICU stay duration will be calculated in days from the day of transplantation until discharge from the ICU.
Unit of Measure: Days Direction: Shorter ICU stay indicates better outcome.
Measured: From the day of liver transplantation until ICU discharge (within 30 days post-transplant).
Hospital Length of Stay
Length of hospital stay after orthotopic liver transplantation will be recorded. Hospital stay duration will be calculated in days from the day of transplantation until hospital discharge.
Unit of Measure: Days Direction: Shorter hospital stay indicates better outcome.
Measured: From the day of liver transplantation until hospital discharge (within 30 days post-transplant).
Postoperative Mechanical Ventilation Duration
Requirement for postoperative invasive mechanical ventilation after orthotopic liver transplantation will be recorded. Prolonged mechanical ventilation is defined as ventilation lasting ≥24 hours.
Unit of Measure: Categorical (prolonged ventilation ≥24 hours vs <24 hours) Direction: Less prolonged mechanical ventilation indicates better outcome.
Measured: From the day of liver transplantation until extubation or 30 days post-transplant, whichever occurs first.
Early Postoperative Complications (within 30 days)
Incidence of early postoperative complications within 30 days after orthotopic liver transplantation will be recorded. Complications include infection, bleeding, biliary complications, and graft dysfunction. Complications will be reported as present or absent and categorized by type.
Unit of Measure: Categorical (present/absent; type-specific) Direction: Fewer complications indicate better outcome.
Measured: Within 30 days after liver transplantation.
30-Day Mortality
Mortality status within 30 days after orthotopic liver transplantation will be recorded.
Unit of Measure: Binary (alive vs deceased) Direction: Lower mortality indicates better outcome.
Measured: Within 30 days after liver transplantation.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Feb 2026
- Study start15 Dec 2025
- Primary completionAug 2026 (estimated)
- Study completionAug 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for End-Stage Liver DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Izmir Bakircay University
- Sponsor type
- University, hospital or other
- Collaborators
- Izmir University of Economics
- Responsible party
- Principal investigator, AYŞE KAYALI VATANSEVER, Izmir Bakircay University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07414095
- Sponsor's protocol ID
- 2537
- Status last verified
- Feb 2026
- First submitted
- 28 Jan 2026
- Last updated
- 17 Feb 2026
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigation of the Relationship Between Frailty, Sarcopenia, Malnutrition, and Psychosocial Parameters and Post-Transplant Outcomes in Liver Transplant Candidates
- ClinicalTrials.gov ID
- NCT07414095
- Acronym / sponsor ID
- 2537
- Conditions
- End-Stage Liver Disease, Liver Transplantation, Cirrhosis
- Keywords
- Liver Transplant Candidates, Frailty, Sarcopenia, Malnutrition, Psychosocial Health
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Izmir Bakircay UniversityUniversity, hospital or other
- Collaborators
- Izmir University of Economics
- Study start
- 15 Dec 2025 (actual)
- Primary completion
- Aug 2026 (estimated)
- Study completion
- Aug 2026 (estimated)
- First posted
- 17 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study will evaluate frailty, nutrition, sarcopenia, and psychological health in people waiting for a liver transplant. The purpose is to understand how these factors affect outcomes before and after transplantation. By identifying patients at higher risk early, the study aims to support the development of better care programs in the future.
Participants will complete simple tests of physical strength, walking speed, and daily activity levels. Their nutrition and psychological well-being will also be assessed. The study will then look at how these results relate to medical scores used in liver disease and to outcomes after transplant, such as hospital stay, complications, or survival.
Adults aged 18-65 years who are on the liver transplant waiting list and can understand Turkish are eligible to join.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Adult Liver Transplant Candidates | – | Other: Comprehensive Observational Assessment in Liver Transplant CandidatesThis cohort includes adult patients (aged 18-65 years) who are on the liver transplant waiting list and able to understand Turkish. Participants will undergo assessments of frailty, sarcopenia, malnutrition, and psychosocial health. No therapeutic intervention will be applied; this is an observational study. Clinical outcomes after transplantation, such as length of ICU stay, hospital discharge time, complications, and survival, will be recorded prospectively. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The study population consists of patients listed as liver transplant candidates at a private hospital in Izmir, Turkey.
Key inclusion criteria (3 listed)
- Being listed as a liver transplant candidate
- Age between 18 and 65 years
- Ability to understand the Turkish language
Key exclusion criteria (4 listed)
- Presence of orthopedic and/or neurological problems severe enough to prevent completion of assessment tools
- Inability to understand verbal commands
- Being a recipient of multiple organ transplants
- Presence of serious active extrahepatic malignancy
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Comprehensive Observational Assessment in Liver Transplant CandidatesThis study involves a comprehensive, multidimensional assessment of liver transplant candidates focusing on frailty, sarcopenia, malnutrition, and psychosocial status. Frailty will be measured using the Liver Frailty Index (LFI), 6-Minute Walk Test (6MWT), Karnofsky Performance Status (KPS), and Activities of Daily Living (ADL). Sarcopenia will be evaluated through handgrip strength, Appendicular Skeletal Muscle Mass (ASM)/Skeletal Muscle Index (SMI), and 4-meter gait speed. Malnutrition will be assessed using the Nutritional Risk Index (NRI) and phase angle derived from bioelectrical impedance analysis. Psychosocial status will be measured with the Hospital Anxiety and Depression Scale (HADS). Clinical parameters (MELD-Na, Child-Pugh, CKI-OKN) will be recorded. Post-transplant adverse outcomes including prolonged hospital and ICU stay, postoperative complications, early mortality, and duration of mechanical ventilation will be monitored up to 30 days after surgery. | Other | Adult Liver Transplant Candidates |
Primary outcome
Liver Frailty Index (LFI)
Time frame: At hospital admission when liver transplantation is confirmed.
Frailty will be assessed using the Liver Frailty Index (LFI), which is calculated from three standardized physical performance tests: grip strength (kg, average of three trials), chair stands (seconds to complete five repetitions), and balance test (seconds, up to 10 seconds in three positions). LFI score will be calculated according to the standard LFI formula. Frailty severity will be categorized as: ≥4.5: Severe frailty 3.2-4.4: Moderate frailty <3.2: Not frail Unit of Measure: LFI score (continuous) Direction: Higher scores indicate greater frailty (worse outcome).
6-Minute Walk Test (6MWT) Distance
Time frame: At hospital admission when liver transplantation is confirmed.
The 6-minute walk test (6MWT) will be conducted according to European Respiratory Society and American Thoracic Society guidelines along a 30-meter corridor. Participants will be instructed to walk as far as possible in six minutes. Distance walked will be recorded in meters and rounded to the nearest meter. Oxygen saturation, heart rate, blood pressure, and fatigue (Modified Borg Scale) will be recorded before and after the test, with continuous SpO₂ and heart rate monitoring during the walk. Frailty classification will be based on the following thresholds: <250 m (severe frailty), 250-350 m (moderate frailty), >350 m (not frail). Unit of Measure: Meters (continuous) Direction: Higher walking distance indicates lower frailty (better outcome).
Karnofsky Performance Status (KPS)
Time frame: At hospital admission when liver transplantation is confirmed.
The Karnofsky Performance Status (KPS) is a subjective measure of frailty, originally developed for oncology and subsequently applied in cirrhosis. The scale ranges from 0% (death) to 100% (normal; no complaints; no evidence of disease), scored in 10-point increments. Applicable to both hospitalized and ambulatory patients. Frailty classification will be based on the following thresholds: 0-40% = Severe frailty 50-70% = Moderate frailty ≥80% = Not frail Unit of Measure: Percentage (%) Direction: Higher KPS score indicates lower frailty (better outcome).
Activities of Daily Living (ADL)
Time frame: At hospital admission when liver transplantation is confirmed.
The Activities of Daily Living (ADL) scale is a subjective measure of frailty, developed to assess functional status in aging populations. It evaluates six functions: bathing, dressing, toileting, continence, transferring, and feeding. The scale is self-reported and scored from 0 (dependent) to 6 (independent). Frailty classification will be based on the following thresholds: ≥2 difficulties (severe frailty), 1 difficulty (moderate frailty), and 0 difficulties (not frail). Unit of Measure: Score (0-6) Direction: Higher scores indicate lower frailty (better outcome).
15 secondary outcomes
Nutritional Risk Index (NRI)
Time frame: At hospital admission when liver transplantation is confirmed.
Phase Angle Measured by Bioelectrical Impedance Analysis (BIA)
Time frame: At hospital admission when liver transplantation is confirmed.
Sarcopenia Diagnosis According to the European Working Group on Sarcopenia in Older People 2 (EWGSOP2) Criteria
Time frame: At hospital admission when liver transplantation is confirmed.
Handgrip Strength (HGS)
Time frame: At hospital admission when liver transplantation is confirmed.
Skeletal Muscle Index (SMI)
Time frame: At hospital admission when liver transplantation is confirmed.
Gait Speed (4-meter walk test)
Time frame: At hospital admission when liver transplantation is confirmed.
Hospital Anxiety and Depression Scale - Anxiety Subscale (HADS-A)
Time frame: At hospital admission when liver transplantation is confirmed.
Hospital Anxiety and Depression Scale - Depression Subscale (HADS-D)
Time frame: At hospital admission when liver transplantation is confirmed.
Hospital Anxiety and Depression Scale - Total Score (HADS Total)
Time frame: At hospital admission when liver transplantation is confirmed.
Charlson Comorbidity Index - Orthotopic Liver Transplant (CCI-OLT)
Time frame: At hospital admission when liver transplantation is confirmed.
Intensive Care Unit (ICU) Length of Stay
Time frame: From the day of liver transplantation until ICU discharge (within 30 days post-transplant).
Hospital Length of Stay
Time frame: From the day of liver transplantation until hospital discharge (within 30 days post-transplant).
Postoperative Mechanical Ventilation Duration
Time frame: From the day of liver transplantation until extubation or 30 days post-transplant, whichever occurs first.
Early Postoperative Complications (within 30 days)
Time frame: Within 30 days after liver transplantation.
30-Day Mortality
Time frame: Within 30 days after liver transplantation.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Feb 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of End-Stage Liver Disease and Liver Transplantation, run by Izmir Bakircay University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 17 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Assistant Professor (14046, ayse.vatansever@bakircay.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Liver Frailty Index (LFI) (time frame: At hospital admission when liver transplantation is confirmed.). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Feb 2026.