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

Sponsor
Indonesia University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06023524
Collaborator
(none)
54
1
2
2.9
18.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Laser Acupuncture and Standard Medication
  • Device: Sham Laser Acupuncture and Standard Medication
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
54 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effectiveness Combination of Laser Acupuncture and Standard Medication on Pain Score, Interincisal Distance and Swelling in Mandibular Third Molar Post-Odontectomy Patients
Anticipated Study Start Date :
Sep 4, 2023
Anticipated Primary Completion Date :
Nov 30, 2023
Anticipated Study Completion Date :
Nov 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Laser 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.

Device: Laser 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

Sham Comparator: Sham Laser Acupuncture and Standard Medication

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

Device: Sham 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

Outcome Measures

Primary Outcome Measures

  1. Visual Analog Scale [Day-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.

  2. Interincisal Space [Day-1 (baseline), Day-3 and Day-7 post-odontectomy]

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

  3. Swelling [Day-1 (baseline), Day-3 and Day-7 post-odontectomy]

    Assess the swelling dimensions using a tape measure

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts 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).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Special dental and oral hospital, Faculty of Dentistry, University of Indonesia Jakarta Pusat DKI Jakarta Indonesia 10430

Sponsors and Collaborators

  • Indonesia University

Investigators

  • Principal Investigator: KEPK FKUI RSCM, The Ethics Committee of the Faculty of Medicine, University of Indonesia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Antonius Hapindra Kasim, doctor, Indonesia University
ClinicalTrials.gov Identifier:
NCT06023524
Other Study ID Numbers:
  • 23-06-0952
First Posted:
Sep 5, 2023
Last Update Posted:
Sep 13, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2023