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Completed

NCT Number: NCT05783011

The Effects of Electroacupuncture on Postoperative Pain

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

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Atatürk University

Erzurum, 25240_, Turkey (Türkiye)

About this study

Postoperative pain is an acute pain that begins with surgical trauma and decreases over time with tissue healing. The level of pain and discomfort felt varies from person to person. The patient's sex and age, physiological and psychological structure, operation area, duration of surgery, premedication, type of anesthetic used, postoperative complications and several other environmental factors can affect this level. After the operation, especially within 48 hours, the pain increases and gradually decreases. Postoperative pain may cause an increase in anxiety and general fear and concern. The stress level caused by surgical trauma in the patient delays recovery and increases mortality and morbidity.

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

electroacupuncture

Procedure

Electroacupuncture was applied bilaterally to the LI4, ST5 and ST6 acupuncture points before and after periodontal flap surgery

Periodontal flap surgery

Procedure

periodontal flap surgery

Primary outcomes

  1. Visual Analogue Scale

    Time frame: 7 days

    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')

Secondary outcomes

  1. Postoperative analgesic requirement

    Time frame: 7 days

    the number of analgesic requirements taken by patients after periodontal surgery.

Sponsors and collaborators

Lead sponsor

Didem OZKAL EMINOGLU

Other

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2022
First posted
Mar 24, 2023
Registry last updated
Mar 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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