The Effects of Electroacupuncture on Postoperative Pain
NCT ID: NCT05783011
Last Updated: 2023-03-28
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
44 participants
INTERVENTIONAL
2021-03-30
2022-12-30
Brief Summary
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The main question it aims to answer is there any efficiacy of electroacupuncture application on postoperative pain reduction.
Participants will get periodontal flap surgery treatment with/without electroacupuncture
Researchers will compare EA and control groups to see if there is any relationship between acupuncture application and postoperative pain
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Detailed Description
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Electroacupuncture (EA) applies electrical stimulation current to needles placed on acupuncture points. It is mainly used to relieve pain and provide operative analgesia.
No study has been found in the literature on the pain-reducing functionality of acupuncture applications in periodontal surgical treatments. In this study, the investigators aimed to examine the effect of electroacupuncture application on the amount of pain felt by patients after periodontal surgery.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
TRIPLE
Study Groups
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EA (electroacupuncture)
Individuals who underwent electroacupuncture before and after flap surgery
Electroacupuncture
Electroacupuncture was applied bilaterally to the LI4, ST5 and ST6 acupuncture points before and after periodontal flap surgery
periodontal flap surgery
periodontal flap surgery
Control
Individuals who have undergone flap surgery only
periodontal flap surgery
periodontal flap surgery
Interventions
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Electroacupuncture
Electroacupuncture was applied bilaterally to the LI4, ST5 and ST6 acupuncture points before and after periodontal flap surgery
periodontal flap surgery
periodontal flap surgery
Eligibility Criteria
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Inclusion Criteria
* pregnancy or breast feeding;
* not receiving anti-inflammatory drug therapy in the last 6 months, chemotherapy or radiotherapy;
* having 6 mm or more probable pocket depth and clinical attachment loss in at least 4 or more teeth when called for control 6 weeks after Phase I treatment
Exclusion Criteria
* pregnant/breastfeeding
* medication for any reason
* smoker/tobacco user
* other periodontal disease other than periodontitis
* chronic inflammatory disease (COPD, asthma)
18 Years
65 Years
ALL
No
Sponsors
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Didem OZKAL EMINOGLU
OTHER
Responsible Party
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Didem OZKAL EMINOGLU
assistant professor
Principal Investigators
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DİDEM ÖZKAL EMİNOĞLU
Role: STUDY_DIRECTOR
Ataturk University
Locations
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Atatürk University
Erzurum, , Turkey (Türkiye)
Countries
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Other Identifiers
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2022
Identifier Type: -
Identifier Source: org_study_id
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