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TENS for Pain and Sleep After Hernia Surgery

NCT07319754 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-01-06

No results posted yet for this study

Summary

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.

Conditions

  • Inguinal Hernia
  • Postoperative Pain
  • Sleep Disturbance

Interventions

DEVICE

Transcutaneous Electrical Nerve Stimulation (TENS)

Physician-supervised application of TENS to the inguinal region after hernia surgery, following a standardized protocol.

OTHER

Standard Postoperative Care

Participants in this arm will receive routine postoperative care following inguinal hernia surgery, without TENS application.

Sponsors & Collaborators

  • Nigde Omer Halisdemir University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-10
Primary Completion
2026-10-01
Completion
2026-10-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07319754 on ClinicalTrials.gov