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RecruitingNCT07077382PANDECTUpdated Jul 22, 2025

Pneumoconiosis and Dust Exposure China Cohort

An observational study in Pneumoconiosis, sponsored by China-Japan Friendship Hospital. Recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2025-07-22.

Sponsored by China-Japan Friendship Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started May 2021; still recruiting 5 years 4 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Sex
All
01

Study summary

The primary objective of this study is to characterize the demographic and clinical features of patients with occupational pneumoconiosis (hereinafter referred to as pneumoconiosis) in China. Secondary objectives include: 1) to describe the natural course of pneumoconiosis; 2) to evaluate the prognosis of pneumoconiosis patients; and 3) to assess complications and comorbidities in pneumoconiosis patients.

02

Conditions studied

  • Pneumoconiosis
03

In context

Lead sponsor

China-Japan Friendship Hospital is the lead sponsor of 173 studies on the registry; 109 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients were selected during physical examinations or during hospitalization from medical organization.

Inclusion criteria

  • Diagnosed as pneumoconiosis

Exclusion criteria

Exclusion Criteria:

  • Incomplete occupational history information
  • Has participated in any interventional clinical research
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Target follow-up
3 Years
Patient registry
Yes

Groups and cohorts

  • Patients with pneumoconiosis

    This group is composed of patients with pneumoconiosis.

  • Dust exposure group

    This group is composed of patients exposed to dust.

  • Healthy control group

    This group is composed of healthy control subjects.

06

What researchers measure

Primary outcomes

  1. Pulmonary function test

    Pulmonary function tests (PFTs) are utilized to assess the severity of the patient's condition, monitor disease progression, guide therapeutic decision-making, and evaluate prognosis.

    Time frame: 3 years

Secondary outcomes

  1. Number of patients

    The researchers used inclusion/exclusion criteria for screening, and collected the demographic information, clinical symptoms and signs, laboratory tests, treatment, survival and other conditions of the patients who agreed to participate in the program and signed the informed consent, and collected biological specimens.

    Time frame: 6 years

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Study locations

1 of 1 sites recruiting
  • China-Japan Friendship Hospital
    Beijing, Beijing Municipality 100029, China
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07077382
Lead sponsor
China-Japan Friendship Hospital
Collaborators
KaiLuan General Hospital, The First Affiliated Hospital of Shanxi Medical University, Weifang Respiratory Disease Hospital, Hubei Hospital of Traditional Chinese Medicine, Hunan Prevention and Treatment Institute for Occupational Diseases, China, The first affiliated hospital of chongqing medical and pharmaceutical college, Centers for Disease Control and Prevention, China, Shandong Gold Mining Company Occupational Disease Precention Hospital, Shandong Province Hospital of occupational diseases, The Second Hospital of Heilongjiang Province
Responsible party
Dai Huaping (Chief physician, China-Japan Friendship Hospital) — Principal investigator
First posted
Jul 22, 2025
Start date
May 28, 2021
Primary completion
Mar 31, 2026 (estimated)
Completion
May 31, 2030 (estimated)
Last update
Jul 22, 2025
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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