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transcutaneous electrical nerve stimulation (TENS) is beneficial for postoperative pain relief following inguinal hernia repair: a randomized placebo-controlled trial

transcutaneous electrical nerve stimulation (TENS) is beneficial for postoperative pain relief following inguinal hernia repair: a randomized placebo-controlled trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609001084279
Enrollment
50
Registered
2009-12-18
Start date
2009-12-24
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Yet, no study has demonstrated the benefits of TENS in treating postoperative pain after inguinal herniorrhaphy using SCL. The research question for this study were: 1. Does TENS applied for 30 minutes twice daily reduce pain intensity and SCL after inguinal hernia repair ?

Interventions

Active TENS group received conventional TENS of 100 Hz, pulse width of 120 microseconds, with perceptible tingling sensation, applied for 30 minutes, twice daily for 5 consecutive days using 2 electrodes that were placed parallel to the incision.

Sponsors

mohammed Taher Ahmed Omar
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment

Eligibility

Sex/Gender
Male
Age
30 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

The inclusion criteria were: (1) direct or indirect inguinal hernia (Gillbert 1989); (2) use of Lichtenstein surgical technique (Lichtenstien and Shulman 1994); (3) infiltration anesthetic technique (Amid et al 1994); (4)male adult aged between 25 and 45 years; (5) physical status I - II, according to American Assoication of anesthesia (ASA ) (Hamza et al., 1999); (6) no hearing, visual, or speaking impairments; (7) no cognitive disturbances; and (8) resident of Cairo, willing to the participate, with support for postoperative care and a telephone at home for medical assistance, if necessary.

Exclusion criteria

Exclusion criteria were: (1) morbid obesity; (2) poor liver (serum bilirubin>2.0 mg/dL) or kidneys (serum creatinine>1.5 mg/dL.) (Chiu et al., 1999);(3) neurological or pulmonary diseases;(4) cardiac illness, such as cardiac arrhythmia, angina pectoris, congestive heart failure, and uncontrolled hypertension, and (5) chronic use of opioids (Chiu et al., 1999).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026