Viewing Study NCT06500390



Ignite Creation Date: 2024-07-17 @ 10:59 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06500390
Status: RECRUITING
Last Update Posted: 2024-07-15
First Post: 2024-07-08

Brief Title: Temporomandibular Disorder in Use of Levonorgestrel Intrauterine System
Sponsor: Marmara University
Organization: Marmara University

Study Overview

Official Title: Is the Incidence of Temporomandibular Disorder Increased in the Use of Levonorgestrel Intrauterine System
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to investigate the possible role of levonorgestrel intrauterine system useLIU in the pathogenesis of temporomandibular joint disorder TMD In this clinical trial levonorgestrel intrauterine system patients n30 aged 25-50 and control group patients n30 with the same demographics and age range are used The main questions it aims to answer are

To compare the frequency of temporomandibular dysfunction in women using the levonorgestrel intrauterine system with the control group of the same demographic and age range

The levonorgestrel intrauterine system use group consisted of 50 women who had previously a mirena implanted by a gynecologist at least 3 months ago due to menstrual bleeding and pelvic pain

The control group included 50 randomised healthy women who had regular menstrual cycles and were not taking any medication
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None