Ignite Creation Date:
2024-05-06 @ 8:19 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06331871
Status:
RECRUITING
Last Update Posted:
2024-03-26
First Post:
2024-02-24
Brief Title:
Effectiveness of US-PENS for Patients With Post-surgical Shoulder Pain
Sponsor:
Universidad Rey Juan Carlos
Organization:
Universidad Rey Juan Carlos
Study Overview
Official Title:
Effectiveness of Ultrasound-guied Percutaneous Electrical Nerve Stimulation US-PENS for Patients With Post-surgical Shoulder Pain
Status:
RECRUITING
Status Verified Date:
2024-03
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 aim of this clinical trial was to demonstrate the effectiveness of the application of ultrasound-guided percutaneous nerve stimulation US-PENS directed at the axillary nerve and the suprascapular nerve in patients with post-surgical shoulder pain
This is a randomized longitudinal prospective and quasi-experimental clinical trial in which a total of 70 patients divided into two groups physiotherapy protocol group n35 and experimental group to which the same protocol was practiced and a US-PENS session was added n35
The intervention and follow-up period of the participants took place over 12 weeks
This is a randomized longitudinal prospective and quasi-experimental clinical trial in which a total of 70 patients divided into two groups physiotherapy protocol group n35 and experimental group to which the same protocol was practiced and a US-PENS session was added n35
The intervention and follow-up period of the participants took place over 12 weeks
Detailed Description:
The objective of this clinical trial is to evaluate the effects of including ultrasound-guided percutaneous nerve stimulation US-PENS on the suprascapular nerve and axillary nerve along with a manual physical therapy protocol in patients with pain and lack of function after a shoulder surgery
Methods 70 patients with shoulder pain undergoing arthroscopic surgery were recruited
They were divided into two groups at random physiotherapy protocol group n35 and experimental group to which the same protocol was practiced and two sessions of US-PENS were added n35
A series of variables were evaluated
Pain disability and functional impotence with the help of the NSPR SPADI and DASH scales
In turn goniometry dynamometry and calculation of the pressure pain threshold were performed
The intervention and follow-up period of the participants lasted 12 weeks
Methods 70 patients with shoulder pain undergoing arthroscopic surgery were recruited
They were divided into two groups at random physiotherapy protocol group n35 and experimental group to which the same protocol was practiced and two sessions of US-PENS were added n35
A series of variables were evaluated
Pain disability and functional impotence with the help of the NSPR SPADI and DASH scales
In turn goniometry dynamometry and calculation of the pressure pain threshold were performed
The intervention and follow-up period of the participants lasted 12 weeks
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?:
False
Is an FDA AA801 Violation?:
None