Comparison of the Effect of Rhythmic Respiration and Lidocaine Spray on the Severity of Arteriovenous Fistula Venipuncture Pain in Patients undergoing hemodialysis
- Conditions
- Severity of Arteriovenous Fistula Venipuncture Pain in Patients undergoing Hemodialysis.Pain from vascular prosthetic devices, implants and grafts, initial encounterT82.848A
- Registration Number
- IRCT20210626051716N1
- Lead Sponsor
- Gonabad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 54
Be between 18 and 60 years old
Willing to cooperate and participate in research
At least 3 months have passed since the fistula was implanted
Lack of pacemaker
Having an active record so that three sessions per week and each session for 4 hours to be treated with Hemodialysis
Absence of skin problems, lack of anesthesia, neuropathic disorders and peripheral vascular diseases at the fistula site
If you have diabetes, have controlled diabetes (FBS samples in the range of 70 to 150 and BS in the range of 120 to 250)
Do not have verbal, visual or auditory impairment
Lack of known allergy to Lidocaine
Do not have drug addiction and dependence on painkillers
Have not received painkillers or sedatives 6 hours before Hemodialysis
Do not have pain in other parts of the body
Do not want to continue collaborating in research
Lack of patient awareness at any stage of the research
Failure of the needle to enter the arteries of the fistula area in the first attempt and the need to repeat the Cannulation
Incidence of Lidocaine sensitivity at any stage of the study
Onset of other chronic pain that affects the assessment of pain due to needle insertion into the fistula
Failure to refer to the research stages (refer to other medical centers to continue treatment, travel, kidney transplant, death)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score in Visual ?Analogue Scale Questionnaire. Timepoint: Evaluation of pain score before the intervention and then three consecutive Hemodialysis sessions in both groups. Method of measurement: Visual Analogue Scale Questionnaire .
- Secondary Outcome Measures
Name Time Method