Ignite Creation Date:
2024-05-06 @ 2:08 AM
Last Modification Date:
2024-10-26 @ 11:14 AM
Study NCT ID:
NCT01979783
Status:
UNKNOWN
Last Update Posted:
2013-11-08
First Post:
2013-10-28
Brief Title:
Correlation Between Electromyography and Thickness Change of the Trunk Muscles in Subjects With Low Back Pain
Sponsor:
University of Belgrade
Organization:
University of Belgrade
Study Overview
Official Title:
None
Status:
UNKNOWN
Status Verified Date:
2013-11
Last Known Status:
NOT_YET_RECRUITING
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:
Transversus abdominis TrA and lumbar multifidus LM muscle have been proposed to play key role in stability of the lumbosacral spine The muscles functional andor structural deficits have been linked to the low back pain LBP syndrome Evaluation of the transversus abdominis and lumbar multifidus muscles function in clinical practice is scarce and not well defined due to number of reasons Surface electromyography of TrA and LM muscles as a method of examining muscles function is not involved in clinical routine Rehabilitative Ultrasound Imaging RUSI of the TrA and LM apart from providing information about their morphology could be helpful in assessing their function Since concentric muscle contraction results in the shortening and thickening of the muscle evaluation of the potential association between muscles morphometry assessed by the ultrasound and electromyography may be of potential clinical interest However this potential relationship is context-dependant Our aim was to establish the difference in the thickness change of the TrA and LM muscle during activation in subjects with and without low back pain and to establish the possible correlation between electromyography and the thickness change of these muscles assessed by ultrasound in both groups of subjects
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None