Single-photon emission computed tomography/computed tomography in patients with a suspected Unilateral Condylar Hyperactivity.

Completed

• Conditions: condylar hyperplasia; 10005959

• Registration Number: NL-OMON39064
• Lead Sponsor: Vrije Universiteit Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

-progressive facial asymmetry with mandible involvement

Exclusion Criteria

-facial asymmetry suspected to be based on a non-UCH cause
-apparent temporomandibular joint disorder
-apparent systemic or local bone disease

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is the sensitivity and specificity of the bone SPECT/CT<br /><br>scan compared to the sensitivity and specificity of the SPECT scan in patients<br /><br>with a suspected UCH. To provide a receiver operating characteristics (ROC)<br /><br>curve in order to select the optimal diagnostic method (SPECT/SPECT-CT). </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The second endpoint of this study is the inter-observer and intra-observer<br /><br>agreement for the SPECT/CT scanning in patients with a suspected UCH</p><br>