Actively Recruiting

Age: 18Years - 70Years
All Genders
ID07280390

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

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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

Diagnostic Evaluation

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

Diagnostic Evaluation

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

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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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