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A randomized controlled clinical trial of blood-pricking and cupping therapy for post-infectious cough

A randomized controlled clinical trial of blood-pricking and cupping therapy for post-infectious cough

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075617
Enrollment
Unknown
Registered
2023-09-11
Start date
2023-02-09
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

cough after infection

Interventions

Experimental group:Basic treatment+ Blood-pricking and cupping
Control group:Basic treatment of cough after infection

Sponsors

The first teaching hospital of Tianjin university of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Meet the above diagnostic criteria of western medicine; ? Age 18-80 years old, gender unlimited; ? Clear awareness, stable vital signs, and cooperation in physical examination; ? VAS is greater than 40mm.

Exclusion criteria

Exclusion criteria: ? Cough or other lung diseases caused by chronic bronchitis, eosinophilic bronchitis, cough variant asthma, gastroesophageal reflux disease, etc; ? Coagulation dysfunction; ? Those who have participated in other clinical trials within one month; ? Women in lactation or pregnancy, or women of childbearing age who plan to be pregnant within 6 months after screening, or women with positive urine pregnancy test; ? Suffering from blood-borne infectious diseases; ? Other conditions that the researcher believes are not suitable to participate in this test.

Design outcomes

Primary

MeasureTime frame
The Leicester Cough Questionnaire;

Secondary

MeasureTime frame
Visual analogue scale;CET;Laboratory indexes;Cough effect;

Countries

China

Contacts

Public Contactxiaoyu Dai

The first teaching hospital of Tianjin university of Chinese medicine

limenghan01@126.com+86 137 0212 0982

Outcome results

None listed

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