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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06001450
Other study ID # STUDY-23-00245
Secondary ID 22-1179-00001
Status Recruiting
Phase
First received
Last updated
Start date August 30, 2023
Est. completion date October 23, 2024

Study information

Verified date September 2023
Source Icahn School of Medicine at Mount Sinai
Contact Mellissa Picker, BS
Phone 212-659-6710
Email mellissa.picker@mssm.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The PLANET Study aims to determine the impact of microplastics on intestinal inflammation and gut microbiome in order to understand the role of this pollutant on the risk of developing inflammatory bowel disease (IBD) as well as other diseases. With this information, the researchers hope to characterize better the role of environmental pollutants on IBD and develop novel strategies towards prevention.


Description:

Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), is a chronic, progressive inflammatory disease of the intestinal tract. The etiology of IBD is not well understood, but believed to result from a complex relationship between genetics, environment, and gut microbiome alterations, resulting in a self-perpetuating, abnormal mucosal immune response. The incidence of IBD is rising in developing and recently developed countries, highlighting the importance of environmental exposures in determining disease risk. Microplastics, defined as plastic particles <5 mm in size, are ubiquitous pollutants with unclear implications towards human health. Emerging studies indicate substantial disruption of intestinal immune function and a proinflammatory milieu due to microplastics. Therefore, identifying, and characterizing microplastics in stool samples of individuals with CD alongside alterations in microbiome and calprotectin, which are events that occur prior to CD onset, is the initial step in exploring the impact of microplastics on IBD. Moreover, CD affects women during their reproductive years and 25% become pregnant after diagnosis. Given that maternal IBD diagnosis is one of the major risks of future IBD in offspring, it is critical to better understand if babies born to mothers with IBD have higher content of microplastics or other toxins in the stools and whether these levels correlate with those of their mothers during pregnancy.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date October 23, 2024
Est. primary completion date October 23, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The ability to sign and date an informed consent form - Be pregnant, or wishing to become pregnant in the near future and enroll the infant that the individual is pregnant with - Aged 18 or older - English-speaking (this observational study uses non-validated questionnaires that are only available in English) - Of any ethnicity - Be a spouse, related household member (sibling, parent, etc.) or a child of an enrolled pregnant person Exclusion Criteria: - Individuals who are unable to give informed consent - Be diagnosed with a pregnancy complication, such as intrauterine fetal demise/stillbirth, preeclampsia, hyperemesis gravidarum, or have an active infection, including chorioamnionitis or sepsis.

Study Design


Locations

Country Name City State
United States Icahn School of Medicine at Mount Sinai New York New York

Sponsors (2)

Lead Sponsor Collaborator
Icahn School of Medicine at Mount Sinai Aalborg University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Microplastics quantification Measuring the concentration, size and shape distributions of microplastics in the stool samples of women with CD, healthy controls and any relatives (spouses and siblings of the infant). 1 year
Secondary Alpha and beta diversity Microbiome characterization - Bacterial DNA will be isolated from stool and sequenced to characterize the bacteria present in the microbiome. Alpha and beta diversity statistics will be reported. 1 year
Secondary Fecal calprotectin analysis Stool samples will be processed to quantify calprotectin levels which are routinely used to characterize inflammation. 1 year
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