Respiratory Functions Response To Tens Acupoint Stimulation Post Inhalation Injury
NCT ID: NCT04667676
Last Updated: 2021-01-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2018-06-10
2019-01-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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TENS Therapy Group
patients received acupoint TENS
acupoint TENS
TENS was applied bilaterally on acupoint Ex-B1, 4Hz frequency, and 200 μs pulse width and intensity was set at the best highest tolerable intensity by the patient sensitivity without a sensation of discomfort for 45 minutes, three times/week for four weeks
Control group
patients received shame acupoint TENS
acupoint TENS
TENS was applied bilaterally on acupoint Ex-B1, 4Hz frequency, and 200 μs pulse width and intensity was set at the best highest tolerable intensity by the patient sensitivity without a sensation of discomfort for 45 minutes, three times/week for four weeks
Interventions
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acupoint TENS
TENS was applied bilaterally on acupoint Ex-B1, 4Hz frequency, and 200 μs pulse width and intensity was set at the best highest tolerable intensity by the patient sensitivity without a sensation of discomfort for 45 minutes, three times/week for four weeks
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of smoke inhalation based on the history of smoke exposure and chest computed tomography (CT)
* Have no systemic disease
* Body mass index less than 30.
Exclusion Criteria
* Cardiac condition
* Rib fracture
* Systemic disease
* Local infection and cigarette or tobacco use
20 Years
40 Years
ALL
No
Sponsors
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Cairo University
OTHER
Responsible Party
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Marwa Eid
assistant professor of physical therapy for surgery
Locations
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Marwa Eid
Cairo, , Egypt
Countries
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Other Identifiers
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4-12-2020
Identifier Type: -
Identifier Source: org_study_id
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