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Effectiveness and safety of Fu’s subcutaneous needling as adjuvant therapy for symptoms after coronavirus disease 2019: A randomized controlled trial

Effectiveness and safety of Fu’s subcutaneous needling as adjuvant therapy for symptoms after coronavirus disease 2019: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067412
Enrollment
Unknown
Registered
2023-01-06
Start date
2023-01-07
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

Novel Coronavirus Pneumonia (COVID-19)

Interventions

Observation group:Basic treatment, including general treatment such as rest, strengthened support treatment, close monitoring of vital signs, oxygen therapy, antibacterial drug treatment, anti COVID-1
control group:Basic treatment, including general treatment such as rest, strengthened support treatment, close monitoring of vital signs, oxygen therapy, antibacterial drug treatment, anti COVID-19 dr

Sponsors

Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Conform to diagnostic criteria of coronavirus disease 2019; (2) The age is more than 45 years old and less than 90 years old; (3) Within one month, the patient was newly infected with COVID-19 and had related clinical symptoms; (4) The vital signs of patients were stable; (5) Sign the informed consent form voluntarily and receive Fus subcutaneous needling.

Exclusion criteria

Exclusion criteria: (1) Body temperature = 37.3 ?; (2) Those who have poor mental status, can not cooperate, or suffer from mental diseases, have no self-control, and can not express clearly, can not accept floating needle treatment, or can not cooperate to complete the efficacy evaluation due to other reasons; (3) Subjects participate in other clinical studies after infection; (4) Accompanied with serious cardiovascular and cerebrovascular diseases.

Design outcomes

Primary

MeasureTime frame
the cough VAS;Evaluation Scale of Therapeutic Effect of Traditional Chinese Medicine on coronavirus disease 2019 (COVID-19);

Secondary

MeasureTime frame
MMrc score;Fatigue Scale-14,FS-14;Inflammatory indicators;CT imaging changes;Hospitalization days;7-day discharge rate;

Countries

china

Contacts

Public ContactBai Tianyu

Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University

baitianyu19820217@163.com+86 15168879181

Outcome results

None listed

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