An experimental study comparing the time of application of warm therapy to reduce pain, anxiety, and side-effects during randomized extraction of patients with chronic renal failure
- Conditions
- Diseases of The genitoruinary system
- Registration Number
- KCT0004264
- Lead Sponsor
- Sunchon National University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 80
Selection Criteria
(1) Those who understand the purpose of this study and agree to participate in the study
(2) Those who have received hemodialysis regularly for more than 3 months in an arteriovenous fistula
(3) An adult patient aged 20 years or older who has no mental deficiencies and can understand and answer the contents of
the experiment,
(4) A person who does not have an inflammatory or dermatological history of the venous puncture site
(5) Patients who do not receive other pain relievers for arteriovenous fistula
Exclusion criteria
(1) complications associated with arteriovenous fistulas, such as surgery or surgery
(2) If you have hypersensitivity reactions and circulatory disorders
(3) Experience with application of on-therapy to puncture site of arteriovenous fistula
(4) When taking pain medication by disease (within 6 hours of pain medication)
When selecting a subject, I will seek advice from a nephrology internist and a nurse.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anxiety;pain
- Secondary Outcome Measures
Name Time Method Side effects