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Validating placebo needle of Fu's subcutaneous needling on a healthy population: a single-blind, randomized controlled trial

Validating placebo needle of Fu's subcutaneous needling on a healthy population: a single-blind, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071489
Enrollment
Unknown
Registered
2023-05-16
Start date
2023-06-05
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

healthy people

Interventions

Sponsors

Shenzhen Baoan Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18-70 years old, male or female. 2. Participants who haven’t received Fu's subcutaneous needling, voluntarily to take part in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those with acute or chronic pain. 2. Taking analgesics or medications inducing abnormal sensation. 3. Diseases causing sensory disturbance or sensory loss; or those with coagulation dysfunction, dermatological disease, cardiovascular and cerebrovascular diseases, diabetes, or with severe systemic diseases of the liver, kidney and hematopoietic system. 4. Those who refuse Fu’s subcutaneous needling intervention or are allergic to metals. 5. Those with alcohol or drug abuse history. 6. The pregnant or lactating women. 7. Health care workers with knowledge or experience of acupuncture. 8. Patients who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Successful blinding rate;

Secondary

MeasureTime frame
Degree of needling pain;Type of needling pain ;Acceptance of needling;

Countries

China

Contacts

Public ContactQingsong Zhang

Shenzhen Baoan Traditional Chinese Medicine Hospital

78654546@qq.com+86 189 2521 3636

Outcome results

None listed

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