Periodontitis Clinical Trial
Official title:
The Effects of Electroacupuncture on Postoperative Pain
NCT number | NCT05783011 |
Other study ID # | 2022 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 30, 2021 |
Est. completion date | December 30, 2022 |
Verified date | March 2023 |
Source | Ataturk University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this study,the investigators aimed to examine the effect of electroacupuncture application on the amount of pain felt by patients after periodontal surgery. 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
Status | Completed |
Enrollment | 44 |
Est. completion date | December 30, 2022 |
Est. primary completion date | December 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - absence of any systemic disease, - 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: - Having a systemic disease such as cardiovascular, diabetes, hypertension, thyroid organ pathologies, chronic kidney failure - pregnant/breastfeeding - medication for any reason - smoker/tobacco user - other periodontal disease other than periodontitis - chronic inflammatory disease (COPD, asthma) |
Country | Name | City | State |
---|---|---|---|
Turkey | Atatürk University | Erzurum |
Lead Sponsor | Collaborator |
---|---|
Didem OZKAL EMINOGLU |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analogue Scale | The Visual Analogue Scale consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be') | 7 days | |
Secondary | Postoperative analgesic requirement | the number of analgesic requirements taken by patients after periodontal surgery. | 7 days |
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