About this trial
This study evaluates whether Transcutaneous Electrical Nerve Stimulation (TENS) improves postoperative pain and sleep quality in adults undergoing inguinal hernia surgery. After surgery, participants will receive physician-supervised TENS or usual care. Pain intensity and sleep quality will be measured and compared between groups to assess the effectiveness and safety of TENS as a supportive recovery method.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults (≥18 years) undergoing elective inguinal hernia surgery
Disqualifiers
History of epilepsy, cardiac pacemaker, or other contraindications to TENS
Trial design
Parallel
Treatments tested in this trial
Transcutaneous Electrical Nerve Stimulation (TENS)
DevicePhysician-supervised application of TENS to the inguinal region after hernia surgery, following a standardized protocol.
Standard Postoperative Care
Other interventionParticipants in this arm will receive routine postoperative care following inguinal hernia surgery, without TENS application.
Treatment groups
Trial outcomes
Primary outcomes
Postoperative Pain Intensity
Pain intensity will be measured using the Visual Analog Scale (VAS) at 6, 12, and 24 hours postoperatively.
Change in Pain Intensity (VAS)
Pain intensity will be measured using the Visual Analog Scale (VAS) at 6, 12, and 24 hours postoperatively.
Sponsors and contacts
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