Adverse Effects of Miniscalpel Needle
Not Applicable
Recruiting
- Conditions
- Not Applicable
- Registration Number
- KCT0002849
- Lead Sponsor
- Cheongyeon Korean Medicine Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
1. Male and female patients aged 18-90 years who received Miniscalpel-Needle therapy at the Chung-Yeon Korean Medicine Hospital (Sang-Mu branch) after the research approval date
2. Those who are able to communicate with researchers with minimal help, and report adverse reactions
3. Those who voluntarily signed the agreement after hearing the explanation of the research after the research approval date
4. If the information such as sex, age, etc. is not missing on the medical records
Exclusion Criteria
1. Patients who are deemed unsuitable for research by researchers
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Observation of adverse effects after Miniscalpel-Needle therapy (Perform necessary tests such as blood test, image test in case of adverse effect after face-to-face surveys, telephone surveys.);calculation of the incidence of adverse effects
- Secondary Outcome Measures
Name Time Method umber of patients per month;Patient drop out rate signed the agreement;Patient drop out rate after treatment;Time required for completing consent and tracking patient calls;Appropriateness of the case report item and clarity of expression;Severity of adverse events(Use Common Terminology Criteria for Adverse Events scale),;Causality of adverse events(Use The World Health Organization-Uppsala Monitoring Centre causality assessment system);NRS (numeral rating scale);Patient satisfaction after treatment (Llikert 5 points scale);Researcher comment as base material of SOP(standing operating procedure) production