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survey about adverse event after acupotomy

Survey for physician about adverse events associated with Acupotomy in real wolrd practice

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0004482
Enrollment
100
Registered
2019-11-28
Start date
2019-11-17
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

None listed

Interventions

None listed

Sponsors

Chung Yeon Korean Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. ?? 2? ?? ??? ??? ???? ??? ????? ? ? ?? ? 2. ?? ???? ???? ?? ??? ?

Exclusion criteria

Exclusion criteria: 1. A person who cannot report all procedures and side effects for at least 2 weeks 2. Others judged by the researcher as inappropriate

Design outcomes

Primary

MeasureTime frame
topical adverse events;systemic adverse events—

Secondary

MeasureTime frame
adverse events causality;severity of adverse events—

Countries

Korea, Republic of

Contacts

Public ContactDamin JEON

Chung Yeon Korean Medicine Hospital

damin2snub@naver.com+82-70-4678-0696

Outcome results

None listed

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