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Clinical study of Th1/Th2 balance drift and Omega-3 fatty acid intervention in people with high PM2.5 exposure in Chengdu subway station hall

Clinical study of Th1/Th2 balance drift and Omega-3 fatty acid intervention in people with high PM2.5 exposure in Chengdu subway station hall

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038065
Enrollment
Unknown
Registered
2020-09-09
Start date
2020-11-01
Completion date
Unknown
Last updated
2020-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Th1/Th2 balance drift in human body under high PM2.5 exposure

Interventions

low exposure group A:Oral mega-3 fatty acids
low exposure group B:Oral placebo
high exposure group A:Oral mega-3 fatty acids

Sponsors

The Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for people with high PM2.5 exposure: (1) The staff in Chengdu Metro Station Hall, male or female, age: 20-65 years old, working in the station hall >= 3 times per week, working time >= 8 hours per day, and working time >= 2 years; (2) Those who have had no obvious abnormalities in the physical examination in the past year; (3) No hormone preparations have been used in the past 3 months; (4) No history of surgery in the past three months; (5) Informed consent to join this experimental study and sign the informed consent form. Inclusion criteria for people with low PM2.5 exposure: (1) The staff in the office of Chengdu Metro Station Hall (air-conditioning device equipped with PM2.5 filters), regardless of gender, age: 20-65 years old, working >= 3 times per week, working hours >= 8 per day Hours, working time >= 2 years; (2) Those who have had no obvious abnormalities in the physical examination in the past year; (3) No hormone preparations have been used in the past 3 months; (4) No history of surgery in the past three months; (5) Informed consent to join this experimental study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those with a long-term history of drug use; (2) Those who have a history of smoking; (3) Those with a history of massive bleeding; (4) Those who are allergic to flaxseed, fish and seafood; (5) Those with a history of hepatitis, fatty liver, cirrhosis, cholecystitis, and gallstones; (6) Those who are pregnant and lactating; (7) Participants in other clinical trials in the past 6 months; (8) Those who cannot understand the intention of this experiment and are difficult to cooperate with the experiment process.

Design outcomes

Primary

MeasureTime frame
Th1 and Th2 cell levels and the ratio of the two;Th1 and Th2 cytokine levels;

Secondary

MeasureTime frame
Levels of IL-4 and INF-? in nasal lavage fluid;IL-8 and ICAM-1 levels in serum;Serum levels of hypersensitivity C-reactive protein;Pulmonary function;SF-36;COOP/WONCA chart;Otolaryngology, Respiratory and Cardiovascular Department Visits and Follow-up Record Form;

Countries

China

Contacts

Public ContactShuiqin Li

The Affiliated Hospital of Chengdu University of Traditional Chinese Medicine

160218115@qq.com+86 18628912226

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026