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NCT04085068 Clinical Trial

Effect of Dural Release on Women With Back and Neck Pain After Obstetrics and Gynecological Surgery

Back Pain Clinical Trial

Official title:
Effect of Dural Release on Women With Back and Neck Pain After Obstetrics and Gynecological Surgery

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04085068
Other study ID # P.T.REC/012/00191
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 8, 2023
Est. completion date November 11, 2023

Study information
Verified date September 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Something must be done in order to release the tension within the dura mater before any lasting correction of the spine can be effected. Each of the cranial nerves is wrapped in a sheath of dura mater. As they exit the cranial vault they are described by Gray's Anatomy as having a "dural cuff".

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date November 11, 2023
Est. primary completion date November 1, 2023
Accepts healthy volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - The age of the participants will be ranged from 20 to 40 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: - Bone disease. Discogenic state with radiculopathy or not. Systemic disease of musculoskeletal system. Any sensory problems. Previous vertebral fractures. Major spinal structural abnormality.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• cranioscaral treatment
dural release

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Outcome
Type Measure Description Time frame Safety issue
Primary body mass index BMI in kg/m^2 3 months
Primary Satisfaction assessed by the VAS Degrees of menstrual pain will be assessed using a VAS, which was a method of representing subjects' pain on a 10 cm linear scale. Score of 0 meant 'no pain' and 10 meant 'worst pain'. Tomeasure specific symptoms 3 months
Primary a pressure-pain threshold algometer Algometers are devices that can be used to identify the pressure and/or force eliciting a pressure-pain threshold. It has been noted in pressure-pain threshold studies that the rate at which manual force is applied should be consistent to provide the greatest reliability 3 months
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