Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01628796
Other study ID # 08-2012.CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 19, 2012
Last updated June 26, 2012
Start date July 2012
Est. completion date January 2013

Study information

Verified date June 2012
Source The Baruch Padeh Medical Center, Poriya
Contact Gordon Edelson, MD
Phone 97246652670
Email edelson@bezeqint.net
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Is it possible to improve the accuracy of injection into the acromio-clavicular joint with the use of ultrasound?


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date January 2013
Est. primary completion date January 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- adults over 18 years with AC joint degenerative changes

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms

  • Osteoarthritis of Acromioclavicular Joint

Intervention

Other:
contrast material injection
using ultrasound to locate ac joint and injecting contrast material to ensure that the dye is actually in the joint

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The Baruch Padeh Medical Center, Poriya

Outcome

Type Measure Description Time frame Safety issue
Primary ultrasound controlled injection of contrast material into the AC joint followed by standard x-ray standard x-ray will be taken after the contrast dye has been injected into the joint to see whether it has successfully been placed into the joint. outcome assessed at the time of the injection (1 day) No