Pain, Postoperative Clinical Trial
Official title:
The Effect of Transcutaneous Electrical Nerve Stimulation (TENS) Application on Patients' Pain Level and Analgesic Use in Patients Undergoing Hip Replacement
The surgical treatment of an individual with osteoarthritis and hip fracture is provided by hip replacement surgery. While restructuring the joint surfaces with surgery, it is aimed to provide both hip joint movements and to treat pain. Intense perioperative pain after hip replacement is common due to inflammatory agents and surgical intervention (eg, involvement of soft tissue and sensory nerves). Inadequately treated acute postoperative pain causes longer hospital stay, limited and delayed bed rest, decreased compliance with physical therapy, and an increased incidence of postoperative complications. It is thought that this method, which can be effective in the pain control of the patient, will be beneficial for the patient both physiologically and psychologically by reducing pain and discomfort. The most important advantage of TENS; It can be easily applied by nurses and easily taught to patients or families. The nurse has a great role in the follow-up of the patient after the surgery, as she/ he is with the patient for 24 hours. When the literature is examined, it is seen that the number of studies showing the effectiveness of TENS application in patients who underwent hip prosthesis, where studies were conducted with patients with knee gonarthrosis, is limited. In this direction, the aim of the study is to examine the effect of TENS application on patients' pain level and analgesic use in patients undergoing hip replacement.
Status | Not yet recruiting |
Enrollment | 60 |
Est. completion date | July 1, 2024 |
Est. primary completion date | December 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - be over 18 years old - hip replacement insertion - not have a pacemaker or arrhythmia - no history of pain, alcohol use or substance abuse - no history of pain, alcohol use or substance abuse - no history of pain, alcohol use or substance abuse - no history of psychiatric illness - no history of metastatic disease - being conscious, able to speak - No barriers to the application of TENS; no postoperative complications - being I, II and III in the ASA classification of the American Society of Anesthesiology, agreeing to participate in the study. Exclusion Criteria: - having a history of epilepsy - Using analgesics at least 1 hour before TENS is applied - the presence of a wound in the area where the electrode will be placed. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Cukurova University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in the pain level using the VAS. | Reducing the pain level of patients undergoing hip replacement by applying TENS.
A value of 0 on the scale means that the patient does not experience pain, and a value of 10 means that he experiences pain at the most severe level |
48 hour | |
Primary | Change in analgesic consumption | Changing analgesic consumption of patients by applying TENS. The analgesic consumption in the first 2 days after the surgery will be learned by using the questionnaire. | 48 hour |
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