Skip to content

Outcomes & Evaluations of Vibration Anesthesia on Cosmetic Botulinum Toxin Injections

Outcomes & Evaluations of Vibration Anesthesia on Cosmetic Botulinum Toxin Injections

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043540
Enrollment
Unknown
Registered
2021-02-21
Start date
2021-02-22
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

Botox injection

Interventions

experimental group:toxin injection under vibration anesthesia
control group:toxin injection without vibration anesthesia

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients who are over 18 years old, who first or repeatedly inject botulinum toxin into masseter muscle, frontal line, eyebrow, nose, mandibular margin, eye corner line, neck line, gastrocnemius muscle, armpit and other parts, who can clearly score according to the pain scale, have good language expression ability, and can clearly express the pain, and have the same botulinum toxin injection requirements in the same parts of both sides of the body.

Exclusion criteria

Exclusion criteria: Patients are who are pregnancy, lactation, menstruation, under 18 years old, allergic to botulinum toxin, infection of injection site, taking analgesics before injection, suffering from neuromuscular diseases. Patients currently use aspirin and other anticoagulants, aminoglycoside antibiotics, magnesium sulfate, quinidine, lincomycin, myenterin and other drugs.

Design outcomes

Primary

MeasureTime frame
Pain assessment;

Countries

China

Contacts

Public ContactYoubai Chen

Chinese PLA General Hospital

807750706@qq.com+86 15110264464

Outcome results

None listed

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