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Not yet recruiting NCT06946147

Assessment of Temporomandibular Joint Function Across Different Trimesters of Pregnancy

Observational Temporomandibular; Functional Disturbance

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Temporomandibular; Functional Disturbance. Basic parameters: 20 years — 35 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study will be conducted to assess Temporomandibular Joint (TMJ) function across different trimesters of pregnancy.

Detailed description

Pregnancy is a physiological state that can potentially influence the function and biomechanics of the Temporomandibular Joint (TMJ) due to hormonal changes, weight gain, and other associated factors. TMJ disorders are a common problem affecting a significant proportion of the population, with potential impacts on chewing, speaking, and other daily functions, significantly affecting a pregnant woman's quality of life.

Limited research has been conducted to comprehensively evaluate the changes in TMJ function and proprioception (repositioning accuracy) across different trimesters of pregnancy. By identifying and understanding the specific impacts of different trimesters of pregnancy on TMJ function, this study aims to provide insights that can help in the early detection and effective management of TMJ disorders. This, in turn, can improve the overall well-being and comfort of pregnant women, contributing to a more positive pregnancy experience.

Moreover, physiotherapists currently have limited guidelines specifically tailored for managing TMJ dysfunction in pregnant patients. This study aims to fill this gap by providing evidence-based insights into the mechanisms and risk factors associated with TMJ dysfunction during pregnancy. The findings can inform the development of clinical guidelines and therapeutic protocols that address the unique needs of pregnant women, ensuring safer and more effective care.

Interventions

  • Other

Primary outcome measures

  • Mouth Opening (Eyes Open) [Time frame: 5 months]
  • Mouth Opening (Eyes Closed) [Time frame: 5 months]
  • Right Lateral Movement (Eyes Open): [Time frame: 5 months]
  • Right Lateral Movement (Eyes Closed) [Time frame: 5 months]
  • Left Lateral Movement (Eyes Open) [Time frame: 5 months]
  • Left Lateral Movement (Eyes Closed) [Time frame: 5 months]
  • Jaw protrusion (Eyes Open) [Time frame: 5 months]
  • Jaw protrusion (Eyes Closed) [Time frame: 5 months]
Secondary outcome measures (2)
  • Assessment of severity of temporomandibular joint dysfunction [Time frame: 5 months]
  • Assessment of temporomandibular joint pain [Time frame: 5 months]

Eligibility criteria

Inclusion criteria

All women will be pregnant with a single baby. Their ages will range from 20 to 35 years old. Their parity will range from 1 to 2. Their body mass index will range from 20 to 30kg2.

Exclusion criteria

All women will not suffer from any TMJ disorder or orofacial pain before pregnancy.

All women will not suffer from any severe dental pathology. All women will not suffer from high-risk pregnancy (hyperemesis gravidarum, gestational diabetes).

All women will not suffer from any systemic illnesses.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Egypt · 1 center
  • Maha Zaghloul mohammed — Cairo

Identifiers

NCT: NCT06946147 · P.T.REC/012/005674

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗