Effect of Marjoram, Vetiver, and Lavender Oil in the Treatment of Bruxism (NCT07665398) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Effect of Marjoram, Vetiver, and Lavender Oil in the Treatment of Bruxism
Turkey (Türkiye)64 participantsStarted 2024-09-02
Plain-language summary
The aim of this study was to investigate the possible effects of the use of lavender, marjoram and vetiver oil via inhalation and/or massage application on the treatment of bruxism.
Who can participate
Age range
18 Years – 25 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* • Patients between 18-25
* Patients with full dentition including 2nd molars
* Patients without facial asymmetry
* Patients without history of sensitivity or allergy to plants
* Patients without olfactory disorders
Exclusion Criteria:
* • Patients with systemic (asthma history) and/or neuromuscular disease
* Patients with orofacial pain not caused by bruxism
* Temporomandibular joint (TMJ) surgery or injection history
* Use of any medical drug affecting the muscular system
* Patients with developmental deformity or surgery history in the maxillofacial region (facial trauma history, resection history, etc.)
* TMJ pathologies (major condylar changes seen on panoramic radiograph)
* Radiotherapy and/or chemotherapy history
* Ongoing orthodontic treatment
* Removable prosthesis use
* Inflammatory connective tissue diseases
* Pregnancy
* Obstructive sleep apnea
* Local skin infection over the myofascial area
* Reluctance to take responsibility for the work
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.