- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05600010
Detection of Microplastics in Cardiac Surgery Patients
Detection of Microplastics in Cardiac Surgery Patients: Its Metabolic Pathways and Toxic Effects
The exponential growth in plastic production/use translates into a parallel increase in environmental plastic waste, which is constantly degraded into microplastics and nanoplastics. Information on the effects of microplastics on human health is still preliminary.
Cardiac surgery patients is a population high exposed to plastics. This observational study will obtain biological samples of cardiac surgery patients as a reference and vulnerable group of individuals highly exposed to microplastics and potentially more susceptible.
The objective of this research is to be able to detect microplastics on blood and operation samples of cardiac surgery patients as well as their potential genotoxic and immunological damage.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Kun Hua, M.D.
- Phone Number: +8615810111206
- Email: huakun0310@126.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age ≥18 years
- Elective cardiac surgery
Exclusion Criteria:
- Emergency surgery or limited-term surgery
- Previous cardiac surgery
- Previous severe liver disease
- Pregnant or planning to become pregnant
- Have a malignant tumor
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Study group
Detection of microplastics/nanoplastics in heart tissue and the blood of patients undergoing cardiac surgery
|
Detection of microplastics as a yes/no value
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Detection of microplastics in human heart tissue and the blood
Time Frame: perioperative: preoperative and pro-/postoperative blood and intraoperative heart tissue
|
Detection of microplastics in human heart tissue and the blood undergoing cardiac surgery
|
perioperative: preoperative and pro-/postoperative blood and intraoperative heart tissue
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Kun Hua, Beijing Anzhen Hospital
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- default
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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