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Effectiveness using of TENS (Transcutaneous Electrical Nerve Stimulation) in pain controlling while change dressing in hospitalized burned patients

Effectiveness using of TENS (Transcutaneous Electrical Nerve Stimulation) in pain controlling while change dressing in hospitalized burned patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014101719561N1
Enrollment
60
Registered
2015-03-17
Start date
2014-05-22
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

burn. Burn of second degree, body region unspecified

Interventions

Intervention 1: Control Group: Before washing the patient’s lesions and exchanging the bandage, 5 mg of Morphine ampoule is infusion and we start to exchange the bandage 15 minutes later and at the la
Treatment - Drugs
Treatment - Devices
Placebo
Control Group: Before washing the patient’s lesions and exchanging the bandage, 5 mg of Morphine ampoule is infusion and we start to exchange the bandage 15 minutes later and at the last, the Patient’
Intervention Group: Before washing the patient’s wounds and exchanging the dress, infusion Morphine ampoule for 5 mg and we start to exchange the bandage 15 minutes later. Morphine ampoule was infusio
Placebo Group: Before washing the patient’s wounds and exchanging the dress, 5 mg of Morphine ampoule is infusion and we start to exchange the dress 15 minutes later. Morphine ampoule was infusion bef

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All of patients with Superficial and deep by grade 2 of burn; The consciousness burned patients to 4-20 range percent; The patients that have 15-70 age old; The burned patients in upper or lower or upper and lower members. Exclusion criteria: The mental retardation patients that don’t talk measure of numeric pain scale; The burned patients less of 4 and more of 20 percent; The pregnant patients (special in third of pregnancy); The patients with heart disorders or have a pace maker; The patients with sensibility to gel; The patients that have an epilepsy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: while intervention(in third days of hospitalization). Method of measurement: measure of numeric pain scale.

Secondary

MeasureTime frame
Skin sensivity to TENS. Timepoint: after of end intervention. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mahtab Khajeh

Sabzevar University of Medical Science

mahtabkhajeh@yahoo.com+98 51 4423 9605

Outcome results

None listed

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