Skip to content

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

The Effectiveness Combination of Laser Acupuncture and Standard Medication on Pain Score, Interincisal Distance and Swelling in Mandibular Third Molar Post-Odontectomy Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06023524
Enrollment
54
Registered
2023-09-05
Start date
2023-09-04
Completion date
2023-10-31
Last updated
2023-11-08

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

Conditions

Impacted Third Molar Tooth, Laser Acupuncture

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.

Interventions

DEVICELaser Acupuncture and Standard Medication

Laser 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

DEVICESham Laser Acupuncture and Standard Medication

Laser Acupuncture: using RJ laser Nogier E program, with 4672Hz, 785 nm and power 70 mW. The laser is turned on but not activated

Sponsors

Indonesia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog ScaleDay-1 (baseline), Day-3 and Day-7 post-odontectomyRating 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.
Interincisal SpaceDay-1 (baseline), Day-3 and Day-7 post-odontectomyAssess the maximum distance of opening the mouth (interincisal space) using calipers
SwellingDay-1 (baseline), Day-3 and Day-7 post-odontectomyAssess the swelling dimensions using a tape measure

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026