Health Condition 1: E888- Other specified metabolic disorders
Conditions
Interventions
Intervention1: Nil: Nil
Intervention2: Nil: Nil
Intervention3: Nil: Nil
Sponsors
Institute of Liver and Biliary Sciences
Eligibility
Inclusion criteria
Inclusion criteria: Diagnosed liver cirrhosis, hospital admission during study period
Exclusion criteria
Exclusion criteria: Acute liver failure or acute on chronic liver failure, hepatic encephalopathy more than grade 1, severe cognitive impairment, recent major surgery within 1 month, pregnant/parturient/breastfeeding women, mechanical ventilation at the time of assessment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the prevalence of pain in patients with liver cirrhosis at the time of hospital admission. Timepoint: At hospital admission | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess pain severity (Numeric Rating Scale) & characteristics Timepoint: At hospital admission;To assess association of pain with neuropathic features (Douleur Neuropathique 4 Questionnaire) Timepoint: At hospital admission;To assess association of pain with decompensation parameters of liver cirrhosis Timepoint: At hospital admission;To assess association of pain with severity of liver disease Timepoint: At hospital admission;To assess association of pain with impact on function (Insomnia- Insomnia Severity Index & quality of life - Chronic Liver Disease Questionnaire) Timepoint: At hospital admission;To assess impact of pain on outcome (ICU admission, duration of hospital stay & 28-day mortality) Timepoint: 28th day of hospital admission;To determine the proportion of patients requiring analgesicsTimepoint: At hospital admission & 28th day of hospital admission | — |
Countries
India
Contacts
Public ContactMahima Agarwal
Institute of Liver and Biliary Sciences, New Delhi
Outcome results
None listed