Temporomandibular Disorder in Use of Levonorgestrel Intrauterine System
Recruiting
N/A
Interventional Study
Levonorgestrel Adverse Reaction
Temporomandibular Joint Disorders
Temporomandibular Disorder
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 100 (estimated)
- Sponsor
- Marmara University · Other
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About This Trial
The goal of this clinical trial is to investigate the possible role of levonorgestrel intrauterine system use(LIU) in the pathogenesis of temporomandibular joint disorder (TMD). In this clinical trial, levonorgestrel intrauterine system patients (n=30) aged 25-50 and control group patients (n=30) with the same demographics and age range are used. The main questions it aims to answer are:
To compa…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Being a woman
* Having used an intrauterine device for at least 3 months
* Being between the ages of 18-50
* Being in American Society of Anesthesiologists-1 and American Society of Anesthesiologists-2 systemic status
Exclusion Criteria:
* Patients with craniofacial syndrome…
Contacts