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Efficacy of Botulinum Toxin and Marjoram Oil Applications in Bruxism

B

Bezmialem Vakif University

Status

Completed

Conditions

Bruxism, Sleep

Treatments

Procedure: Clinical evaluation
Procedure: Imaging Time
Procedure: Aromatherapy
Procedure: Botox administration

Study type

Interventional

Funder types

Other

Identifiers

NCT06674733
13.02.2024-E.140948

Details and patient eligibility

About

Objective: Bruxism is defined as clenching or grinding teeth unconsciously. It can be categorized under two subheadings: sleep and awake bruxism. This study aims to investigate the effectiveness of botox applications, a current approach in the treatment of sleep bruxism, and to evaluate the effectiveness of alternative therapies like aromatherapeutic oils. The study will compare and assess the efficacy of these methods.

Materials and Methods: This prospective study will be conducted between March 2024 and January 2025 at Bezmialem Vakıf University, Faculty of Dentistry, Department of Oral and Maxillofacial Radiology, with patients aged between 18 and 60 who have presented complaints of clenching/grinding teeth, sleep bruxism, jaw, neck, or face pain, and insomnia. The patients diagnosed with sleep bruxism will be divided into two groups, each consisting of 15 patients. The first group will include 15 patients with sleep bruxism who will receive botulinum toxin-A (BTX-A) injections, and the second group will consist of 15 patients who will use marjoram oil as an alternative treatment. Ultrasound imaging will assess the thickness and stiffness of the masseter muscle before treatment, and at 1 and 3 months post-treatment. Clinical evaluations will also be performed before treatment, and at 1 and 3 months post-treatment using scoring systems.

Enrollment

30 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Self-reported teeth clenching or grinding
  2. Tenderness or fatigue in the masticatory muscles upon palpation
  3. Increased morning muscle pain
  4. Localized myofascial pain in the jaw, face, or neck region
  5. Irregular or excessive enamel wear consistent with bruxism
  6. Grinding sounds during sleep confirmed by a partner
  7. Morning jaw muscle stiffness and spasms causing sleep disturbances
  8. Individuals older than 18 years,
  9. Individuals younger than 60 years,
  10. Provided informed voluntary consent

Exclusion criteria

  1. Botulinum toxin injection into the masseter muscle within the last 6 months
  2. Use of night guards
  3. Pathology or history of surgery involving the masseter muscle or parotid gland
  4. Benign or malignant tumors in the mandibular region
  5. History of alcohol or substance abuse
  6. Age below 18 or above 60
  7. Pregnancy, postpartum period, or breastfeeding
  8. Infection or dermatological lesions at the injection site
  9. Diagnosis of chronic obstructive pulmonary disease (COPD) or asthma
  10. Known allergy or skin reaction to botulinum toxin A or essential oils used in aromatherapy
  11. Use of muscle relaxants or other medications that may affect muscle function

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Botox group
Active Comparator group
Description:
Group 1 will consist of patients with bruxism complaints who are indicated for botox treatment and will receive BTX-A.
Treatment:
Procedure: Botox administration
Procedure: Imaging Time
Procedure: Clinical evaluation
aromatherapy group
Active Comparator group
Description:
Group 2 will consist of patients with bruxism complaints and will receive Origanum Majorana (marjoram oil)
Treatment:
Procedure: Imaging Time
Procedure: Aromatherapy
Procedure: Clinical evaluation

Trial contacts and locations

1

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Central trial contact

Elifhan Alagoz, Asst. Prof.

Data sourced from clinicaltrials.gov

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