Skip to content

The effect of electrical stimulation on pressure injuries: double-blind controlled cross over study.(Verification by double blind crossover comparison test.)

The effect of electrical stimulation on pressure injuries: double-blind controlled cross over study.(Verification by double blind crossover comparison test.) - The effect of electrical stimulation on pressure injuries: double-blind controlled cross over study.(Verification by double blind crossover comparison test.)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029516
Enrollment
20
Registered
2017-10-13
Start date
2017-12-07
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Pressure injury

Interventions

The subjects are divided into sham group or stimulation group after observation for one week. Sham stimulation (0 mA) is took on the wound in the sham group, and monophasic pulsed micro-current (0.17

Sponsors

Housenka Hospital
Lead Sponsor
Kobe Gakuin University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) The patients with the pressure injury of National Pressure Ulcer Advisory Panel pressure injuries stage 2, 3 or 4 2) The patients who are expected to hospitalize for more than one month. 3) The patients who have pressure injury for more than one month. 4) The patients who consent in writing in person or representative.

Exclusion criteria

Exclusion criteria: 1) The patients with a malignant tumor. 2) Severe infection in pressure injury. 3) Patients with arterial/ venous thrombosis or thrombophlebitis. 4) Patients with unstable general condition such as high fever above 38.0 degrees. 5) Patients who cannot keep the electrodes on the wound. 6) Patients who develop a feeling of anxiety about the electrical stimulation. 7) Patients who the primary doctor or dermatologist judge the subjects.

Design outcomes

Primary

MeasureTime frame
Wound contraction Compare the rate of wound contraction between sham period and electrical stimulation period. Compare the wound contraction ratio in the current stimulation period of two weeks and the wound contraction ratio in the two weeks sham stimulation period.

Secondary

MeasureTime frame
DESIGN-R Observation of wound Clinical blood test Adverse events (anthema, redness, dysesthesia as itch sensation, pain, heat sensation, and abnormal sensation as oppressing feeling)

Countries

Japan

Contacts

Public ContactTerutaka Hiramatsu

Housenka Hospital Department of Rehabilitation

rihaptot@seiwa-h.org072-641-7063

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026