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Effect of preoperative percutaneous electrical nerve stimulation on severity of postoperative pain

Comparison of preoperative percutaneous electrical nerve stimulation on intensity of pain surgery in patient under inguinal herniorrhaphy in case and control groups

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012102311228N1
Enrollment
66
Registered
2013-01-03
Start date
2012-11-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Pain. Pain localized to other parts of lower abdomen

Interventions

Intervention 1: In the case group one hour before the surgery TENS device EV-906 model made in Taiwan is connected to the incision site by the interviewer number 1. Sensory intensity is activated in t
Treatment - Devices
Placebo
In the case group one hour before the surgery TENS device EV-906 model made in Taiwan is connected to the incision site by the interviewer number 1. Sensory intensity is activated in the range of 9 to
In the control group one hour before the surgery TENS device EV-906 model made in Taiwan is connected to the incision site by the interviewer number 1. The indicator light is on but the device is inac

Sponsors

Vice Chancellor for research, Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Male, aged 20 to 50, suffering from inguinal hernia; Use of Liechtenstein surgical procedure; Surgery performed in the morning to avoid circadian cycle; Physical status of ASA I or II; Absence of hearing, visual or talking impairment; Lack of cognitive impairment; No exclusion criteria Exclusion criteria: Conditions prohibiting the use of TENS, (such as pacemakers, because of the unknown effects of TENS on electrical conduction system or placing the electrode directly on open wounds); Obesity (weight more than 100 pounds above ideal weight); Recurrent, incarcerated and bilateral hernia; Skin infection or severe skin disease in the place of the electrodes; Chronic use of narcotics or antidepressant drugs

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The surgical site pain. Timepoint: 2, 4, 6, 12 and 24 hours after the surgery. Method of measurement: Using the visual analog scale method.

Secondary

MeasureTime frame
Vomitting. Timepoint: 2, 4, 6, 12 and 24 hours after the surgery. Method of measurement: Asking the patient.;Nausea. Timepoint: 2, 4, 6, 12 and 24 hours after the surgery. Method of measurement: Asking the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Monir Janzamini

Kashan University of Medical Sciences

janzamini@kaums.ac.ir+98 36 1555 0026

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026