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"Effect of Transcutaneous Electrical Nerve Stimulation in pain controlling Orthopedic Patients"

• Comparison of the Effectiveness of Transcutaneous Electrical Nerve Stimulation in Control the pain intensity of postoperative Orthopedic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171007036612N2
Enrollment
160
Registered
2017-12-01
Start date
2017-12-06
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

The Relationship of Effect of Nervous-Stimulated Nervous Stimulation on the Control of Post-Operative Orthopedic Patients' Pain.

Interventions

Intervention 1: Intervention group 1: The HIGH TENS group in this group uses the Total TENS EMS 2015 to set the frequency to 100 Hz and intensity of 10-30 MA. For each person only once, for 30 minutes
Intervention group 1: The HIGH TENS group in this group uses the Total TENS EMS 2015 to set the frequency to 100 Hz and intensity of 10-30 MA. For each person only once, for 30 minutes. To stimulate,
Intervention group 2: The LOW TENS group in this group uses the Total TENS EMS 2015 device to set the frequency to 10 Hz and the intensity of 50-20 mA. For each person only once, for 30 minutes. To s
Intervention group 3 : The BURST group in this group uses the Total TENS EMS 2015 device to set the settings to 1_2 pulse circuits with a frequency of 100 Hz and low current. For each person only once
Control group: routine care is provided to control  patient's pain

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All orthopedic patients more than 18 years old, who have pain after orthopedic surgery

Exclusion criteria

Exclusion criteria: Having a pacemaker and Cardiac arrhythmia pregnant women

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before intervention immediately after intervention. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMotahareh Farshad Faghih

Zahedan University of Medical Sciences

motahareh_farshadfaghih@yahoo.com+98 31 3332 8590

Outcome results

None listed

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