MedPath

The Effectiveness of Laser Acupuncture and Standard Medication Therapy on Mandibular Post-Odontectomy Patients

Not Applicable
Completed
Conditions
Laser Acupuncture
Impacted Third Molar Tooth
Interventions
Device: Sham Laser Acupuncture and Standard Medication
Device: Laser Acupuncture and Standard Medication
Registration Number
NCT06023524
Lead Sponsor
Indonesia University
Brief Summary

Acute toothache is a problem that often occurs in the oral cavity. Toothache can be caused by an impacted tooth, in which the tooth cannot or will not erupt into its normal position. The American Association of Oral and Maxillofacial Surgeons (AAOMFS) states that 9 out of 10 people have at least one impacted tooth, and impacted mandibular third molars have the greatest prevalence. Laser acupuncture is an acupuncture modality that has the benefit of reducing pain after third molar extraction. The goal of this randomized controlled trial is to evaluate the group that received a combination of laser acupuncture and standard medication compared to the group that received the combination of sham laser acupuncture and standard medication alone, in management of post-mandibular odontectomy patients. The main objective of this study is to analyze the combination of laser acupuncture and medication significantly improving the patient's pain intensity, interincisal distance and post-odontectomy swelling compared to the combination group of sham laser acupuncture and medication.

Detailed Description

This is a clinical trial study to evaluate the group that received a combination of laser acupuncture and standard medication compared to the group that received the combination of sham laser acupuncture and standard medication alone, in management of post-mandibular odontectomy patients. The required sample was 57 mandibular third molars in male/female subjects post-odontectomy and randomized into 2 groups: (1) combination of laser acupuncture with standard medication and (2) combination of sham laser acupuncture with standard medication. The subjects will receive two times treatment, on day-1 (baseline) and day-3 after odontectomy. The outcome will be assessed on day-1 (baseline), day-3 and day-7 post-odontectomy. Patients and outcome assessors will be blinded to the group allocation.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Male or female subject
  • Age 18 - 40 years
  • Classification of Pell and Gregory class I, II and positions A, B, C
  • Willing to participate in this research and sign informed consent
Exclusion Criteria
  • Pregnancy
  • Have a history of using corticosteroid drugs in the last 3 months
  • Have a history of medication with analgesics at least 24 hours before surgery
  • Have an unstable systemic disease (such as uncontrolled hypertension and diabetes etc.)
  • The patient has a medical emergency / hemodynamically unstable (such as having a hypertensive crisis)
  • Wounds or skin diseases at the location of the acupuncture point irradiation
  • Patients with a history of epilepsy
  • High fever (> 38oC).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sham Laser Acupuncture and Standard MedicationSham Laser Acupuncture and Standard MedicationSham Laser Acupuncture: using RJ laser Nogier E program, with 4672Hz, 785 nm and power 70 mW. The laser is turned on but not activated
Laser Acupuncture and Standard MedicationLaser Acupuncture and Standard MedicationLaser Acupuncture: using RJ laser Nogier E program, with 4672Hz, 785 nm and power 70 mW. Dose 4 Joule at the acupuncture body points and 1 Joule at the ear points.
Primary Outcome Measures
NameTimeMethod
Visual Analog ScaleDay-1 (baseline), Day-3 and Day-7 post-odontectomy

Rating scale for measuring pain, where the minimum value is 0 = no pain, and the maximum value is 100 = severe pain. A higher scale means worse outcomes.

SwellingDay-1 (baseline), Day-3 and Day-7 post-odontectomy

Assess the swelling dimensions using a tape measure

Interincisal SpaceDay-1 (baseline), Day-3 and Day-7 post-odontectomy

Assess the maximum distance of opening the mouth (interincisal space) using calipers

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Special dental and oral hospital, Faculty of Dentistry, University of Indonesia

🇮🇩

Jakarta Pusat, DKI Jakarta, Indonesia

© Copyright 2025. All Rights Reserved by MedPath