CompletedNot Applicable

Cone Beam CT for Diagnosis of Select Otorhinolaryngology (ENT) Indications at Lower Dose

United States, Belgium, France96 participantsStarted 2012-09-21

Plain-language summary

The study objective is to compare the CBCT images generated by the CS 9300 to those generated by conventional CT.

Who can participate

Age range18 Years – 80 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Subject must be 18-80 years of age * Subjects has provided informed consent * Subjects must present with symptoms and/or pathology of the sinus or temporal bone region. * Subject scheduled for additional radiological follow-up and/or endoscopy/surgery. * CBCT exam performed within a maximum of 2 days of the conventional CT. Exclusion Criteria: * Subjects under the age of 18 years, or over the age of 80 years * Unable to collect all required case information * Subjects not willing to consent, or consent is withdrawn * Women in pregnancy or suspected of being pregnant confirmed by pregnancy test

What they're measuring

Percentage of Participants With >=3 Diagnostic Rating Using Radlex Scale

Timeframe: 11 months

Trial details

NCT IDNCT01855425

SponsorCarestream Health, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2013-08-09

Results submitted2017-07-12

View on ClinicalTrials.gov More CerebroSpinal Fluid (CSF) Leak trials