Viewing Study NCT06503302



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06503302
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-07-10

Brief Title: The Effect of Doppler Ultrasound on Calcified Tendinitis
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Doppler Ultrasound on Calcified Tendinitis a Double Blind Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Calcific tendinitis of the shoulder is a self-limiting disease characterized by the deposition of calcium phosphate crystals in the rotator cuff tendons Patients will develop complications such as decreased range of motion of the shoulder joint and thus reducing their quality of life The most common site of occurrence is 15-2 cm away from the supraspinatus tendon insertion site on the greater tuberosity The primary treatment for calcific tendinitis is conservative such as non-steroidal anti-inflammatory analgesics for pain relieving extracorporeal shock wave therapy subacromial steroid injections ultrasound-guided barbotage technique for aspirating and washing out calcific deposits Ultrasound is being used in calcified tendinitis for evaluating its size location quality and also using the color Doppler ultrasonography to evaluate its reactive inflammatory changes However the use of color Doppler ultrasonography in diagnosing and treating a shoulder pain with calcification is not being concluded yet Therefore the aim of this study is to evaluate the efficacy of color Doppler ultrasonography in calcified tendinitis
Detailed Description: Purpose To evaluate the efficacy of color Doppler ultrasonography in calcified tendinitis

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