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Efficacy of Sildenafil in the Improvement of Cognition and Quality of Life in Patients With Cirrhosis of Liver. A Proof of Concept Study.

To Study The Proof of Concept in The Improvement of Cognition and Quality of Life in Cirrhotic Patients With Minimal Hepatic Encephalopathy by Means of a Pharmacological Intervention With Sildenafil (A Phosphodiesterase-5 Inhibitor).

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02028429
Enrollment
50
Registered
2014-01-07
Start date
2012-07-31
Completion date
2014-01-31
Last updated
2014-01-07

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

Conditions

Hepatic Encephalopathy.

Keywords

Minimal Hepatic Encephalopathy (MHE), Psychometric Hepatic Encephalopathy Score (PHES), Sickness Impact Profile (SIP), Model for End-stage Liver Disease (MELD), Child-Turcotte-Pugh score (CTP)

Brief summary

The study is being conducted to evaluate the efficacy of Sildenafil (a 5-phosphodiesterase inhibitor) as a means to improve the cognitive impairment encountered in patients of minimal hepatic encephalopathy (MHE) as proposed in different studies. This study would also assess the role of improvement of cognition as a means of improvement in quality of life.The patients will receive Sildenafil or no treatment for 4 weeks. This study may prove and provide important therapeutic strategy for cognition impairment in patients with MHE.

Detailed description

Primary Aim 1. To study the proof of concept in the improvement of impairment in cognition as assessed by PHES (psychometric hepatic encephalopathy score) in patients of MHE by means of pharmacological intervention by Sildenafil (a phosphodiesterase(PDE)-5 inhibitor) before and after treatment. 2. To study the impact of treatment with Sildenafil administration on the improvement in health-related quality-of-life of patients as assessed by Sickness impact profile (SIP) before and after treatment. Secondary Aim 1. To study the impact of treatment with Sildenafil on CTP and MELD scores before and after treatment. 2. To study the impact of treatment with Sildenafil on blood ammonia and Interleukin-6 levels before and after treatment. Study Population: The study population comprises of male adult (age 18-70 years) with cirrhosis of liver. Patients with cirrhosis of liver have been divided into two groups - with MHE and without or no MHE (NMHE) based on the test result of PHES, i.e., abnormal (MHE group) or normal (NMHE group). Inclusion Criteria: * Male patients aged 18-70 years diagnosed to have cirrhosis of liver at Liver Clinic of Department of Hepatology, Postgraduate Institute of Medical Education & Research(PGIMER), Chandigarh by means of clinical, biochemical and ultrasonographical/CT or liver biopsy. * MHE will be defined by PHES ≤-5 and normal Mini-Mental State Examination (MMSE) score of ≥24. Exclusion Criteria: * Patients unable to give informed consent. * H/O alcohol intake during last 12 weeks. * Significant comorbid illness such as heart disease, respiratory disease, or renal failure. * Any neurological disease such as Alzheimer disease, Parkinson's disease, stroke, non- hepatic metabolic encephalopathy's. * Any anatomical deformities or disease of the penis such as Peyronie's disease. * Patients having psychiatric illness and taking treatment with antidepressant, sedative or neuroleptics. * Patients who start taking alcohol during the study period will be excluded. * Patients taking vasodilators such as nitrates. * Hepatocellular carcinoma. * Recent history of upper GI bleed in last 6 weeks. * Active ongoing infection. * Electrolyte abnormality precipitating MHE. * Color vision abnormalities.

Interventions

DRUGSildenafil.

Arm 1 :Sildenafil Drug Dosage: 25 mg once a day for one week followed by 25 mg twice daily for two weeks then 25 mg thrice daily for one week.

Sponsors

Post Graduate Institute of Medical Education and Research, Chandigarh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

• Male patients aged 18-70 years diagnosed to have cirrhosis of liver at Liver Clinic of Department of Hepatology, PGIMER Chandigarh by means of clinical, biochemical and ultrasonographical/CT or liver biopsy. * MHE will be defined by PHES ≤-5 and normal MMSE score of ≥24.

Exclusion criteria

* Patients unable to give informed consent. * H/O alcohol intake during last 12 weeks. * Significant comorbid illness such as heart disease, respiratory disease, or renal failure. * Any neurological disease such as Alzheimer disease, Parkinson's disease, stroke, non- hepatic metabolic encephalopathy's. * Any anatomical deformities or disease of the penis such as Peyronie's disease. * Patients having psychiatric illness and taking treatment with antidepressant, sedative or neuroleptics. * Patients who start taking alcohol during the study period will be excluded. * Patients taking vasodilators such as nitrates. * Hepatocellular carcinoma. * Recent history of upper GI bleed in last 6 weeks. * Active ongoing infection. * Electrolyte abnormality precipitating MHE. * Color vision abnormalities.

Design outcomes

Primary

MeasureTime frameDescription
Cognition( PHES)4 weeksImprovement of impairment in cognition as assessed by PHES (Psychometric Hepatic Encephalopathy Score) in patients of MHE (Minimal hepatic Encephalopathy) by means of pharmacological intervention by sildenafil (a PDE-5 inhibitor) before and after treatment.
QOL(SIP)4 weeksTo study the impact of treatment with sildenafil administration on the improvement in health-related quality-of-life of patients as assessed by sickness impact profile (SIP) before and after treatment.

Secondary

MeasureTime frameDescription
CTP and MELD score before and after treatment with Sildenafil.4 weeksTo study the impact of treatment with sildenafil on CTP and MELD scores before and after treatment.
Blood Ammonia and Interleukin-6 levels before and after treatment with Sildenafil.4 weeksBlood Ammonia and Interleukin-6 levels before and after treatment.

Countries

India

Outcome results

None listed

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