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Pulmonary ultrashort wave therapy for COVID-19 infection: a single-blind, multi-center randomized controlled clinical study

Pulmonary ultrashort wave therapy for COVID-19 infection: a single-blind, multi-center randomized controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067904
Enrollment
Unknown
Registered
2023-01-31
Start date
2023-01-31
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

COVID-19 Infection

Interventions

Ultrashort wave treatment group:Lung ultrashort wave therapy+conventional therapy
Control group:Conventional therapy

Sponsors

Affiliated Rehabilitation Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The age is 18-80 years old; 2. According to the diagnostic criteria of China's Diagnosis and Treatment Plan for COVID-19 Infection (Tenth Edition on Trial), the patient was diagnosed as COVID-19 infection; 3. According to the clinical typing criteria of the China's Diagnosis and Treatment Plan for COVID-19 Infection (Tenth Edition on Trial), the patients were identified as moderate or severe patients; 4. Vital signs are stable; 5. The patient and his/her family members voluntarily informed and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients requiring intensive care or mechanical ventilation; 2. There are metal implants in the upper torso; 3. Abnormal sensation in chest or upper back skin; 4. People with cardiac pacemaker in the body; 5. Patients with body temperature>38.5 ?; 6. Pregnant or lactating women; 7. Patients with active hemorrhage, uncontrolled active tuberculosis and malignant tumor; 8. Other pathogens (such as tuberculosis and mycoplasma) are positive.

Design outcomes

Primary

MeasureTime frame
CT improvement;White blood cell count;Lymphocyte percentage and count;C-reactive protein;Calcitonin;Neutrophil percentage and count;Blood gas analysis;Interleukin 6;SIRS score;Lung function test;6 min walking test;Borg Dyspnea Score;Respiratory muscle function test;global rating of change scales;

Secondary

MeasureTime frame
General vital indicators and symptoms;drug use;Ultrashort wave related adverse events;

Countries

China

Contacts

Public ContactFeng Zen

the Fourth Affiliated Hospital of Nanchang University

fengzhenly@sina.com+86 13970038111

Outcome results

None listed

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