the Study of Persistent Organic Pollutants in Human Milk

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT04102085
Collaborator
(none)
50
1
25
2

Study Details

Study Description

Brief Summary

The study aims to recruit eligible participants and conduct interviews, collect human milk samples, and conduct laboratory analysis of persistent organic pollutants' levels in human milk samples.

Condition or Disease Intervention/Treatment Phase
  • Other: no intervention

Detailed Description

Persistent Organic Pollutants (POPs) are a group of chemicals which have been intentionally or inadvertently produced and introduced into the environment. Due to their stability and transport properties, they are widely distributed around the world, and are even found in places where they had never been used, such as the arctic regions. Given their long half-lives and fat solubility, POPs tend to bioaccumulate in animals, particularly in long-lived species at the top of the food-chain. POPs appear at higher concentrations in fat-containing foods, including fish, meat, eggs and milk. POPs are also present in the human body and traces can be found in human milk. The most commonly mentioned POPs are organochlorine pesticides, such as DDT, industrial chemicals, most notably polychlorinated biphenyls (PCBs), and by-products, especially polychlorinated dibenzodioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs). As a group, POPs are of concern for both the environment and human health 1.

With the ratification of the Stockholm Convention on POPs in early 2004, the international community signaled its commitment to reduce or eliminate production and emission of POPs into the environment and ultimately, the human body. There were 12 POPs initially listed under the Convention in 2004 2. The Convention is effective to the People's Republic of China, including the Hong Kong Special Administrative Region (HKSAR). The Environmental Protection Department (EPD) coordinates the HKSAR Government's efforts for the Convention and prepared the HKSAR Implementation Plan 3, in which the Department of Health (DH) is required to conduct the regular local monitoring of POPs in human milk.

The first study of POPs in human milk by DH was conducted during 2008 to 2011, which was made reference to Guidelines for Developing a National Protocol of the Fourth World Health Organization (WHO) - Coordinated Survey of Human Milk for POPs in Cooperation with United Nations Environment Programme (UN Environment) (2007) 4.

Results of the first study by DH was published in a scientific journal 5 and submitted to EPD, which were also discussed in the HKSAR Implementation Plan for the Stockholm Convention on POPs (2016) 5. Compared to the related earlier local studies 7,8,9 conducted by local universities, levels of POPs in human milk had declined over time.

Mothers should be reassured that breast milk is naturally the superior food for infants. The study is intended to provide data to evaluate the effectiveness of the international agreement, i.e. the Stockholm Convention, which aims to reduce the levels of certain POPs in our environment.

The study will also support national capabilities for monitoring and sound management of POPs.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
the Study of Persistent Organic Pollutants in Human Milk
Actual Study Start Date :
Sep 25, 2019
Anticipated Primary Completion Date :
Sep 25, 2021
Anticipated Study Completion Date :
Oct 25, 2021

Arms and Interventions

Arm Intervention/Treatment
Mothers under 30

no intervention will be administered

Other: no intervention
no intervention

Outcome Measures

Primary Outcome Measures

  1. Amount of persistent organic pollutants in breast milk [2 years]

    Approximately 30 types of persistent organic pollutants will be tested

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 30 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Primiparae;

  • 30 years of age or below;

  • Have normal pregnancy;

  • Breastfeeding one infant only, and not multiple pregnancy;

  • Resided in Hong Kong for at least 10 years immediately before the date of interview;

  • Available for sample collection within 3 to 8 weeks of delivery; and

  • Both mother and child should be apparently healthy and free from any known infectious or other diseases (e.g. clinical hepatitis, AIDs, HIV).

Exclusion Criteria:
  • participants with previously diagnosed major diseases such as hepatitis, AIDS and other such diseases shall be excluded from the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bonnie Kwok Hong Kong Hong Kong 000

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Principal Investigator: Lap Ah Tse, Chinese University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tse Lap Ah, Associate professor, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT04102085
Other Study ID Numbers:
  • DH/SEB/NCD/18/2018-19
First Posted:
Sep 25, 2019
Last Update Posted:
Dec 16, 2020
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Dec 16, 2020