Severity of Arteriovenous Fistula Venipuncture Pain in Patients undergoing Hemodialysis. Pain from vascular prosthetic devices, implants and grafts, initial encounter
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria
Exclusion criteria: 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)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| "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 ". | — |
Countries
Iran (Islamic Republic of)
Contacts
Gonabad University of Medical Sciences