Change of Range of Motion of TMJ After Correction of Pelvic a Symmetry in Women With Cyclic Pelvic Pain

Pelvic Pain Clinical Trial

Official title:

Change of Range of Motion of TMJ After Correction of Pelvic a Symmetry in Women With Cyclic Pelvic Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04077788
• Other study ID #: P.T.REC/012/001889
• Status: Completed
• Start date: November 8, 2019
• Est. completion date: August 11, 2020

Study information

• Verified date: September 2022
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Clinical experiences have shown that significant pain regression during a menstrual cycle has been often achieved by the use of spinal manipulative therapy (SMT) indicated in women with primary dysmenorrhea with coexisting functional disorders of lumbosacral (LS) spine. Namely, by activation of the nociceptive and vegetative system, LS spine disorders, before all segmental dysfunction and degenerative changes, can induce referred pain and reflex disturbances of pelvic organs (somatovisceral reflexes). Since significant improvement or disappearance of pain during a menstrual cycle is often achieved with adequate therapy of coexisting vertebral disorders in women with primary dysmenorrhea, it is important to recognise latent or manifest vertebral disorders in dysmenorrheic women using clinical examination (Grgić, 2009).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: August 11, 2020
• Est. primary completion date: August 1, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 20 Years to 40 Years

Eligibility

Inclusion criteria:

• The age of the participants will be ranged from 25 to 35 years.

• Their body mass index will be ranged from 20 to 25 kg/m2.

• They will have regular menstrual cycle.

• They will not receive any hormonal therapy or taking any regular drugs.

Exclusion criteria:

The potential participants will be excluded if they meet one of the following criteria:

• Pelvic inflammatory diseases.

• Any pelvic pathological condition

Related Conditions & MeSH terms

• Pelvic Pain

Intervention

Other:
• muscle energy technique
Muscle energy technique: Application of MET for bone of pelvis: I) Pubis: Cranial Os pubis. Caudal os pubis. II) ileum: Anterior ileum. Posterior ileum. External Rotation (In flare) Lesion. Internal Rotation (Out flare) Lesion. III) sacrum: Forward torsion of sacrum. Backward torsion of sacrum. Muscle energy technique for specific muscles of pelvis and spine: Stretch of the Psoas Major. Stretch of the paravertebral muscle. Stretch of the piriforms.

Locations

Country	Name	City	State
Egypt	Rovan Elbesh	Giza

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Weight-Height Scale	It will be used for measuring the body weight and height of each patient participating in the study to calculate the patient's body mass index (BMI).; Body mass index (BMI) = Weight (Kg	3 months
Primary	Visual analogue scale (VAS)	ain will be assessed by visual analogue scale. It is 10 cm horizontal line with one end described as (no pain=0) and other end (worst pain=10). It was considered a valid way for assessing pain. It allowed graphic representation and numerical analysis of collected data (Boonstra et al., 2008) (Appendix III).	3 months
Primary	Menstrual Distress Questionnaire (MDQ)	The MDQ is a 46-item self-report inventory for use in the assessment and treatment of premenstrual and menstrual symptoms. The MDQ can distinguish cyclical from noncyclical changes in physical symptoms, mood and behavior, and arousal.	3 months
Primary	jaw movement	Maximal vertical mouth opening (MIO): From sitting position, with the use of the calliper, the distance between the incisal edges along the midline of the upper and lower central incisors without pain was measured, by placing one end of the poley gauge against the incisal edge of one of the upper central incisors, and the other end against the incisal edge of the opposing lower incisor.; The distance recorded in millimeters, the subjects was instructed to" open your mouth as wide as possible without causing pain or discomfort". The poley gauge was sterilized with antiseptic solution before and after each measur	3 months