Pain Assessment of a new bloodletting device: A study protocol for a randomized, controlled, double-blind, matched-paired clinical trial
Not Applicable
Recruiting
- Conditions
- Not Applicable
- Registration Number
- KCT0004478
- Lead Sponsor
- Cheonan Korean Medicine Hospital of Daejeon University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
(1) 19-64 year old male and female
(2) Able to collect blood on the same finger of both hands
(3) Subject who agrees to participate in the study and signs the informed consent form
(4) Those who can communicate smoothly and express pain
Exclusion Criteria
(1) Those with blood clotting disorders, such as hemophilia or leukemia
(2) Those who have structural disorders such as defects or deformations in the blood collection area
(3) Those who should avoid blood stimulation due to wounds, skin diseases, etc.
(4) Those with sensory disorders in the area of blood collection, such as hemiplegia or peripheral nerve damage
(5) Any other researcher deemed inappropriate for this test
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS(Visual Analog Scale)
- Secondary Outcome Measures
Name Time Method VRS(Verbal Rating Scale)