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Liver CirrhosistransplantNCT07777705

Application of Different Scores in Predicting Outcomes of Cirrhotic Patients Awaiting Liver Transplantation

An observational study of Liver Cirrhosis and Liver Transplant, run by Assiut University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

the goal of this observational study is to apply different scores 1. To assess Fatigue, Frailty, Liver Transplant Comorbidity Index and MELD 3.0 in patients with liver cirrhosis awaiting liver transplantation. 2. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Liver Cirrhosis, Liver Transplant
How many people
153 participants
Where
No sites listed yet
Study dates
1 Sep 2026to 1 Jan 2028
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 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Study population: cirrhotic patients awaiting transplantation

Who may be able to join

  • • All patients with liver cirrhosis (whatever the etiology) eligible for liver transplantation above the age of 18.
  • Written informed consent provided.

Who cannot join

  • Old age (above 60 years old)
  • Acute liver cell failure without underlying cirrhosis
  • Absolute contraindications (e.g., uncontrolled sepsis, severe cardiopulmonary dysfunction, active malignancy).
  • Extra-MELD indications (e.g., hepatopulmonary syndrome, refractory ascites, cholestatic pruritus, hepatoblastoma). We restricted our cohort to patients listed for liver transplantation based on MELD-driven indications. This decision was made to reduce heterogeneity and ensure that eligibility determinations were primarily driven by MELD scores, thereby allowing us to isolate the relative contribution of frailty in the context of MELD-based allocation

About this study

the goal of this observational study is to apply different scores 1. To assess Fatigue, Frailty, Liver Transplant Comorbidity Index and MELD 3.0 in patients with liver cirrhosis awaiting liver transplantation.

  1. To evaluate the predictive accuracy of these Scores for the short-term outcomes (early complications, recurrent hospitalization and 3-month mortality). 3. To determine whether using these Scores in the pre-transplant evaluation improves risk stratification compared to MELD score alone.
Read the detailed description
  1. Sample Size Calculation: Sample size was calculated using Epi Info 7. According to the results of a previous study (put ref.), frailty was detected in 17% of patients undergoing liver transplantation. Based on this percentage, with a confidence limit of 5%, a confidence level of 90%, and a design effect of 1, the estimated sample size required is approximately 153 patients.

All patients recruited in the current study will be subjected to the following:

  1. Detailed history taking such as age, sex, duration of disease, etiology of liver cirrhosis, endoscopic history, complications, previous hospitalization and indication for liver transplantation.
  2. Laboratory investigations: CBC (Complete Blood Count), Liver Function Test, Kidney Function test, Serum Electrolytes levels (Sodium, Potassium and Calcium).
  3. Calculation of - Child Pugh score . Figure (I) Child Pugh score
  • MELD score = 10 x (0.957 x Ln (serum creatinine mg/dl) + 0.378 x Ln (serum bilirubin mg/dl) + 1.120 x Ln (INR) + 0.643).
  • MELD-Na score = MELD + 1.59 x (135 - Na) with maximum and minimum Na of 135 and 120 mmol/l, respectively.
  • MELD 3.0 = 1.33 if female+4.56 * loge(bilirubin) + 0.82*137 - Na- 0.24* 137 - Na *loge(bilirubin) + 9.09*loge (INR) + 11.14*loge(creatinine) + 1.85*3.5 - albumin- 1.83*3.5 -albumin *loge(creatinine) +6
  1. Anthropometric measurement:
  2. Weight in Kilograms (Kg).
  3. Height in Meters (m).
  4. Body Mass Index in (kg/m2): BMI was calculated as weight (kilograms) divided by height squared (meters) in kg/ m2 with normal range in adult between 18.5 - 24.9 kg/m2 .
  5. Waist Circumference in Centimeters (cm).
  6. Mid-arm circumference in Centimeters (cm).
  7. Fatigue Severity Assessment (via FSS and BFI):
  • Fatigue Severity Scale (FSS) (1 = strongly disagree, 7 = strongly agree).
  • Brief Fatigue Inventory (BFI) (Rating from 0-10).
  1. Fatigue Severity Scale (FSS):

The FSS is a 9-item scale designed to assess the severity of fatigue and its impact on daily activities. Here are the items:

  1. I am easily fatigued.
  2. Fatigue interferes with my physical functioning.
  3. Fatigue causes frequent problems for me.
  4. Fatigue interferes with my ability to work, study, or engage in social activities.
  5. Fatigue interferes with my family life.
  6. Fatigue interferes with my leisure activities.
  7. When I am fatigued, I have difficulty concentrating.
  8. Fatigue is a problem for me.
  9. Fatigue interferes with my ability to maintain a regular exercise program. Scale will be from 9-63. Scale up to 35: no fatigue. Scales >35: severe fatigue.

II) Brief Fatigue Inventory (BFI):

The BFI includes 3 questions on fatigue severity and 6 on how fatigue interferes with daily activities. Here are the items:

Fatigue Severity:

  1. How would you rate your fatigue right now?
  2. How would you rate your usual fatigue over the past 24 hours?
  3. How would you rate your worst fatigue over the past 24 hours? Interference with Daily Activities:
  4. Fatigue interferes with general activity.
  5. Fatigue interferes with mood.
  6. Fatigue interferes with walking ability.
  7. Fatigue interferes with normal work (including housework).
  8. Fatigue interferes with relations with other people.
  9. Fatigue interferes with enjoyment of life.
  10. Liver Transplant Comorbidity Index: This index includes the following components and their respective points Factor Points Coronary artery disease 6 Frailty (LFI more than 4.5) 5 HCC 5 Cr more than 1.0mg/dl or on dialysis 3 Diabetes 1

Total score = sum of points.

  • Low risk: Few or no factors → ~93% 3 year survival.
  • Moderate risk: Intermediate score → ~87% 3 year survival.
  • High risk: Multiple factors → ~80% 3 year survival.
  1. Liver frailty index (LFI): The Liver Frailty Index (LFI) is the most widely validated frailty assessment tool in LT. It integrates three performance-based measures: handgrip strength, the Five-Times Sit-to-Stand Test (5xSST), and balance testing, to generate a continuous score that categorizes patients as robust, prefrail, or frail. The LFI has been shown to independently predict waitlist mortality, hospitalization, and delisting, even after adjustment for MELD score
  2. Handgrip strength:

Handgrip strength is measured using a calibrated handheld dynamometer. Three measurements are obtained from the dominant hand, and the maximum value (in kilograms) is used for scoring. Grip strength reflects global muscle strength and correlates closely with sarcopenia and adverse clinical outcomes in patients with Cirrhosis.

  1. Five-times sit-to-stand test (5xSST):

The Five-Times Sit-to-Stand Test, also referred to as chair-stand time, is a standardized, performance-based measure of lower extremity muscle strength, power, and functional mobility. The test is simple, rapid, and requires no specialized equipment, making it particularly well suited for use in patients with chronic liver disease and LT candidates. The 5xSST is performed as follows: the patient is seated upright in a chair; on command, the patient stands up fully and then sits down completely; this cycle is repeated five times as quickly as possible. The total time is recorded in seconds.

  1. Balance testing:

Balance testing evaluates postural stability and neuromuscular coordination, which are frequently impaired in patients with cirrhosis due to sarcopenia, peripheral neuropathy, and hepatic encephalopathy. Within the LFI, balance is assessed using three hierarchical standing positions that are performed sequentially and held for up to 10 s each.

The three components of the LFI are combined using a validated formula: LFI = (0.330 ×sex-adjusted grip strength in kg) + (0.529 × 5xSST in seconds) + (0.040 × balance time in seconds) + 6.

(calculator available at http://liverfrailtyindex.ucsf.edu).

7.Sarcopenia assessment will be done for those prepared for transplantation: Definition of sarcopenia is based on: -

  1. Computed tomography-skeletal muscle index (CT-SMI) with cut-offs of < 41 cm2/m2 for men and < 32 cm2/m2 for women
  2. Hand grip strength with cut-offs of < 27 kg in men and < 16 kg in women
  3. Bioimpedance analysis-skeletal muscle index (BIA-SMI) with cut-offs of < 8.87 kg/m2 for men and < 6.42 kg/m2 for women . According to guideline for European working group on sarcopenia in older people (EWGSOP, the Sarcopenia Working Group) sarcopenia identification was based on both low muscle mass and strength using CT-SMI and hand grip strength
  • Imaging for assessment of Sarcopenia using:
  1. Computed tomography (CT scan): The CT scanner differentiated body tissues; organs, adipose, skeletal muscle and bone, water and air based on tissue-specific attenuation values such as SM (-29, +150) and adipose tissue (-190, -30). These attenuation values were reported in Hounsfield Units (HU) named after Sir Godfrey Newbold Hounsfield, the scientist and electrical engineer who invented the CT scanner .The L3 region contains the spinal vertebrae, intestine, kidney and liver, in addition to visceral adipose, subcutaneous adipose and seven muscle groups; the psoas, erector spinae, quadratus lumborum, transversus abdominus, external and internal obliques and rectus abdominus Step-by-step Guidelines for analyzing a single cross-sectional image:
  2. Extraction of CT images: The electronic medical record was assessed to determine if the patient of interest had a CT study that included the L3 region during the desired time interval. Once the CT study had been verified, the patient medical record number, CT study type, scan date and storage device (if transporting images) was provided to the radiologist .
  3. Technique for assessment of waist circumference (WC) and skeletal muscle (SM) area Once the L3 image was obtained and determined to be of good quality, the following CT imaging protocol was used for assessment of waist circumference (WC) and skeletal muscle (SM) area at the L3 region. Computed tomography-based assessment at the level of the third lumbar vertebra (L3) is widely regarded as the reference standard for quantitative muscle assessment in patients with cirrhosis and LT candidates. CT uses tissue-specific X-ray attenuation values, expressed in Hounsfield units (HU), to distinguish skeletal muscle, adipose tissue, and bone .Commonly used CT-derived metrics include the psoas muscle area (PMA), psoas muscle index (PMI), and skeletal muscle index (SMI), the latter typically expressed as cross-sectional area divided by height squared (cm²/m²)
  4. Abdominal ultrasound (US): Abdominal ultrasound examinations were performed with the subject in the supine position using a 3.75-MHz convex Ultrasound probe. After the routine screening for the abdomen, a transverse scan at the right groin area demonstrated a cross-sectional view of the right iliac artery and vein, which was used as the landmark to detect the iliopsoas muscle located outside the vessels . The iliopsoas muscle area was measured by manual tracing on the image. The iliopsoas muscle index (IP index) was determined by the muscle area divided by the square of height (m2) .
  5. Bioimpedance analysis (BIA):

Bioimpedance analysis (BIA) involved passage of a small AC electrical current through the body. As current was conducted by body water, impedance was inversely related to total body water, thus allowing calculation of total muscle mass, which was the largest water-rich tissue in the body .Body composition was assessed with bioimpedance analysis (BIA) using Body Composition Analyzer Fat free mass was measured by BIA and skeletal muscle mass (SMM) was calculated by the following equation: SMM (kg) = 0.566 x FFM (fat free mass) Skeletal muscle mass index (SMMI) was calculated as skeletal muscle mass (kg) /height (m)2.

Keywords
cirrhosis and transplantation, Liver cirrhosis, Liver transplantation
Medical subject headings
Liver Cirrhosis, Fibrosis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Waitlist morbidity and Mortality of liver transplantation

    • Risk of early complications, rehospitalization and death while awaiting transplantation.
    1. Post-Transplant Survival for liver transplant recipients
    • 3- month survival (short-term outcome). Mortality hazard ratios associated with frailty, comorbidities, and MELD 3.0

    Measured: 1.5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Aug 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Dec 2027 (estimated)
  4. Study completion1 Jan 2028 (estimated)

Resources

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
153 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07777705
Sponsor's protocol ID
04-2026-100516
Acronym
transplant
Status last verified
Aug 2026
First submitted
7 Aug 2026
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • 1) Peng JK, et al: The impact of cirrhosis on health-related quality of life. Liver International, 2019,39(3), 1234-1242. 2) Alberts CJ, Clifford GM, Georges D, et al (2022): Worldwide prevalence of hepatitis B virus and hepatitis C virus among patients with cirrhosis at country, region, and global levels: a systematic review. Lancet Gastroenterol Hepatol;7(8): 724-735. 3) Bodzin AS, Baker TB: Liver transplantation today: where we are now and where we are going. Liver Transplant: Off Publicat American Assoc Stud Liver Diseas Int Liver Transplant Soc 2018;24:1470-5. 4) Terrault NA, Francoz C, Berenguer M, Charlton M, Heimbach J: Liver transplantation 2023: status report, current and future challenges. Clin Gastroenterol Hepatol : Offi Clin Pract J American Gastroenterol Assocn 2023;21: 2150-66. 5) Hughes CB, Humar A: Liver transplantation: current and future. Abdominal Radiol 2021;46:2-8. 6) Sousa Da Silva RX, Weber A, Dutkowski P, Clavien PA: Machine perfusion in liver transplantation. Hepatology (Baltimore, Md) 2022;76:1531-49. 7) Hoare M, Das T, Alexander G: Ageing, telomeres, senescence, and liver injury. J Hepatol 2010;53:950-61. 8) Saiman Y, Serper M: Frailty and sarcopenia in patients pre- and post-liver transplant. Clin Liver Dis 2021;25:35-51. 9) Zaccherini G, Weiss E, Moreau R: Acute-on-chronic liver failure: definitions, pathophysiology and principles of treatment. JHEP Report :Iinnovat Hepatol 2021; 3:100176. 10) Angeli P, Gines P: Hepatorenal syndrome, MELD score and liver transplantation: an evolving issue with relevant implications for clinical practice. J Hepatol 2012;57: 1135-40. 11) Lai JC, Feng S, Terrault NA, Lizaola B, Hayssen H, Covinsky K: Frailty predicts waitlist mortality in liver transplant candidates. Am J Transplant 2014;14:1870-9. 12) Sinclair M, Poltavskiy E, Dodge JL, Lai JC: Frailty is independently associated with increased hospitalisation days in patients on the liver transplant waitlist. World J Gastroenterol 2017;23:899

Questions about this trial

What is this clinical trial studying?

An observational study of Liver Cirrhosis and Liver Transplant, run by Assiut University.

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 2 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: opening soon, as of the sponsor's last update on 20 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Waitlist morbidity and Mortality of liver transplantation (time frame: 1.5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07777705, which also lists 1 linked publication.

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 20 Aug 2026.

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