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Evaluation of the Efficacy and Standardization of Electrical Press-Needle for Preventing and Managing Postoperative Pain Following Mandibular Wisdom Tooth Extraction

Evaluation of the Efficacy and Standardization of Electrical Press-Needle for Preventing and Managing Postoperative Pain Following Mandibular Wisdom Tooth Extraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000271
Enrollment
Unknown
Registered
2026-02-03
Start date
2026-02-28
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

postoperative pain

Interventions

Electric needle group 1(PRCT):Electric needle(3Hz)
Electric needle group 2(PRCT):Electric needle(3/15 Hz)
Control Group(PRCT):No-Intervention
Electric needle group(RCT):Electric needle
Fake needle group(RCT):False Electric needle

Sponsors

Department of Stomatology, Tianjin Integrated Traditional Chinese and Western Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Individuals meeting the diagnostic criteria who require removal of mandibular wisdom teeth, aged 18–60 years, regardless of gender; (2) Healthy individuals (ASA Class I–II), without significant systemic diseases, capable of tolerating tooth extraction surgery and related procedures, with all preoperative physiological indicators within normal ranges; (3) Individuals who have signed informed consent forms.

Exclusion criteria

Exclusion criteria: (1) Acute inflammatory phase of mandibular wisdom tooth; (2) Use of any medication within 24 hours prior to surgery that may alter pain assessment, such as analgesics or anti-inflammatory drugs; (3) Pregnant, menstruating, or lactating women due to risks associated with surgery, anesthesia, and potential adverse effects of rescue medications; (4) Individuals with allergic constitution or known drug allergies; (5) Patients on long-term anticoagulant therapy, with a history of bleeding, or with any clinical indications thereof; (6) Severe hypertension, recent myocardial infarction, frequent angina attacks, cardiac function class III–IV, or patients with heart disease complicated by hypertension; (7) Patients with hyperthyroidism, acute hepatitis, malignant tumors, or neuropsychiatric disorders; (8) Patients with diabetes, acute renal disease, or those receiving long-term corticosteroid therapy; (9) Individuals unsuitable or contraindicated for acupuncture or electroacupuncture treatment; (10) Individuals who participated in other clinical studies within the past three months.

Design outcomes

Primary

MeasureTime frame
The probability of not needing to take painkillers after surgery;

Secondary

MeasureTime frame
Visual Analogue Scale,VAS;Usage of painkillers;VAS at 2, 4, and 6 hours postoperatively;Oral Health Impact Profile,OHIP;

Countries

China

Contacts

Public ContactWang Fang

Gui Yongli

448273840@qq.com+8615902252191

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026