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A clinical trial for the effect of halo therapy in the rehabilitation treatment of pneumoconiosis

A clinical trial for the effect of halo therapy in the rehabilitation treatment of pneumoconiosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015891
Enrollment
Unknown
Registered
2018-04-27
Start date
2016-11-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

pneumoconiosis

Interventions

Control group:conventional treatment
Treatment group:conventional treatment and halotherapy(1 hour / day, 4 weeks)
pneumoconiosis phase I treatment group:conventional treatment and halotherapy(1 hour / day, 4 weeks)
pneumoconiosis phase I control group:conventional treatment
pneumoconiosis phase II treatment group:conventional treatment and halotherapy(1 hour / day, 4 weeks)
pneumoconiosis phase II control group:conventional treatment
pneumoconiosis phase III treatment group:conventional treatment and halotherapy(1 hour / day, 4 weeks)
pneumoconiosis phase III control group:conventional treatment
Pneumoconiosis combined with COPD treatment group:conventional treatment and halotherapy(1 hour / day, 4 weeks)
Pneumoconiosis combined with COPD control group:conventional treatment
Pneumoconiosis without COPD treatment group:conventional treatment and halotherapy(1 hour / day, 4 weeks)
Pneumoconiosis without COPD control group:conventional treatment

Sponsors

BEIDAIHE SANATORIUM OF CHINESE COAL MINERS (Institute of Occupational Disease Prevention and Treatment, Beidaihe, State Administration of Work Safety)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged 30-85 years old; (2) Patients were diagnosised by pneumoconiosis diagnostic criteria GBZ 70-2015; (3) According to GOLD 2015 copd diagnosis standard, the spirometric diagnosis of post-bronchodilator ratio of FEV1 to FVC of <70%, clinical features cough, sputum, dyspnea etc.; (4) Voluntary participation, signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients combined with active pulmonary tuberculous or suffering from infectious diseases; (2) acute respiratory infections; (3) other server diseases affect cardiopulmonary function (including heart disease with decompensation of heart function).

Design outcomes

Primary

MeasureTime frame
cough symptoms score;expectoration symptoms score;COPD assessment test (CAT);quality of life score;MVV%pred(predicted value);FVC%pred(predicted value);FEV1/FVC;white blood cell count;red blood cell count;hemoglobin concentration;Eosinophil count;Monocyte count;platelet count;Serum ALT level;Serum AST level;Serum ALP level;C-reactive protein level;sputum interleukin-6 level, IL-6;sputum interleukin-8 level, IL-8;sputum tumour necrosis factor-a level, TNF-a;serum interleukin-4 level, IL-4;serum interleukin-8 level, IL-8;serum Interferon-?, IFN-?;serum Insulin-like Growth Factor-1, IGF-1;serum Insulin-like Growth Factor-2, IGF-2;serum Immunoglobulin E, IgE;serum Nitric oxide synthase, NOS;

Countries

China

Contacts

Public ContactChen Gang

BEIDAIHE SANATORIUM OF CHINESE COAL MINERS (Institute of Occupational Disease Prevention and Treatment, Beidaihe, State Administration of Work Safety)

cg710121@126.com+86 13333355897

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026