Efficacy of TEAS On Prevention of Propofol Injection Pain in Children
NCT ID: NCT05296187
Last Updated: 2025-02-17
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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RECRUITING
NA
60 participants
INTERVENTIONAL
2025-02-14
2025-05-30
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
PREVENTION
DOUBLE
Study Groups
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GROUP TEAS
Patients will receive TEAS bilaterally at two acupoints: Hegu (L14) and Neiguan (PC6).
TEAS
Transcutaneous electrical acupuncture stimulation
Control Sham Group
Patients in the sham group will be undergoing electrode attachment on the target acupoints without electronic stimulation.
TEAS
Transcutaneous electrical acupuncture stimulation
Interventions
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TEAS
Transcutaneous electrical acupuncture stimulation
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* patients who have renal, hepatic, cardiac, neurological, psychiatric disease
* Cardiac and cranial surgery
* Pacemaker,
* Emergency surgery and patients requiring rapid serial induction
6 Years
13 Years
ALL
Yes
Sponsors
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Konya Meram State Hospital
OTHER
Responsible Party
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Betul Kozanhan
Ass.Prof.
Locations
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Betul Kozanhan
Konya, , Turkey (Türkiye)
Countries
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Facility Contacts
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Other Identifiers
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TEAS Propofol Injection Pain
Identifier Type: -
Identifier Source: org_study_id
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