Actively Recruiting
The Impact of Microplastics and Nanoplastics on Liver Health and Cardiovascular Diseases in India
Led by Post Graduate Institute of Medical Education and Research, Chandigarh · Updated on 2026-05-15
30
Participants Needed
2
Research Sites
3 weeks
Total Duration
On this page
Sponsors
P
Post Graduate Institute of Medical Education and Research, Chandigarh
Lead Sponsor
V
Vellore Institute of Technology University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating the presence and impact of microplastics (MPs) and nanoplastics in patients with liver cirrhosis and portal hypertension. These plastics, common pollutants found in the environment and some medical products, may accumulate in organs such as the liver, kidneys, and intestines, potentially contributing to liver inflammation, disease progression, and complications. The study aims to compare MPs in patients with cirrhosis to those without liver disease and to understand their effects on liver fibrosis, portal hypertension, cardiovascular, and metabolic functions. The study involves assessing liver tissue samples from patients with cirrhosis who are undergoing elective surgery or liver transplantation. Researchers will analyze the types, sizes, and locations of MPs deposited in the liver, using histopathology and electron microscopy. They will also identify different polymer types of MPs and evaluate plastic exposure through patient history including diet, medications, and medical procedures. Participants will undergo tissue sampling during their surgical procedures or biopsies. The study will include detailed assessments of liver tissue to detect and characterize MPs, as well as blood tests to measure micronanoplastics. Researchers will monitor clinical features such as complications of cirrhosis and collect detailed patient histories. The primary outcome is the analysis of MPs in liver tissue, comparing cirrhosis patients to controls. The study will continue through enrollment and elective endoscopy visits for exposure assessment.
CONDITIONS
Brief Title
Microplastics, Cirrhosis and Portal Hypertension
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 70 years
- Diagnosis of cirrhosis confirmed by histology or clinical, laboratory, and ultrasound findings
- Scheduled for elective surgery or liver transplantation
You will not qualify if you...
- Presence of hepatocellular carcinoma (liver cancer)
- Pregnancy or breastfeeding
- HIV infection or receiving retroviral therapy
- Prior liver treatments such as locoregional therapy or previous abdominal surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - At time of elective surgery or liver transplantation
Participants undergo tissue sample collection and histopathological assessments to detect and analyze microplastics in liver tissue, including their morphology, size, and composition.
1 visit (in-person) during scheduled surgery or transplantation
Duration - At the time of elective endoscopy
Participants provide detailed history related to diet, medication, and prior interventions to assess plastic pollution exposure, including prior biopsy and endoscopy.
1 visit (in-person) during elective endoscopy
Duration - At enrollment
Assessment of micronanoplastics in peripheral blood samples collected to complement tissue analysis.
1 visit (in-person)
Trial Site Locations
Total: 2 locations
1
Dr. Madhumita Premkumar
Chandigarh, Chandigarh, India, 160012
Actively Recruiting
2
PGIMER Chandigarh
Chandigarh, Chandigarh, India, 160012
Actively Recruiting
Research Team
M
Madhumita Premkumar, MD DM
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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