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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04672187
Other study ID # EC-60-237-131
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2017
Est. completion date November 1, 2019

Study information

Verified date December 2020
Source Prince of Songkla University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to assess the accuracy of preoperative HRCT of the temporal bone combined with the preoperative audiologic assessment compared with the intraoperative endoscopic middle ear finding.


Description:

The information of the preoperative HRCT scanning of the middle ear cavity in cholesteatoma combined with the preoperative audiologic assessment could be informed the intraoperative middle ear finding in the patients who were diagnosed with chronic otitis media with cholesteatoma, which influence the plan of surgical management. Whether these preoperative assessments can predict the intraoperative finding is unclear. The aim of this study is to assess the accuracy of preoperative HRCT of the temporal bone combined with the preoperative audiologic assessment compared with the intraoperative endoscopic middle ear finding.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date November 1, 2019
Est. primary completion date November 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - The patients included in this study had otorrhea, hearing loss, or aural fullness that last more than 3 months. Otological examination revealed tympanic membrane perforation or retraction, along with cholesteatoma. Exclusion Criteria: - Patients who had a previous temporal bone fracture, concomitant with congenital craniofacial anomalies, or underwent previous otologic surgery were excluded.

Study Design


Locations

Country Name City State
Thailand Faculty of Medicine, Prince of Songkla University Hat Yai Songkhla

Sponsors (1)

Lead Sponsor Collaborator
Prince of Songkla University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary predictive factor of intraoperative endoscopic finding from preoperative ct finding and preoperative audiological assessment the association of preoperative ct finding and preoperative audiological assessment compared with intraoperative endoscopic middle ear finding in middle cholestaetoma 2 years
Secondary accuracy between preoperative ct finding and intraoperative endoscopic finding accuracy between preoperative ct finding and intraoperative endoscopic finding of middle ear cholesteatoma 2 years
See also
  Status Clinical Trial Phase
Completed NCT04489550 - How Long Must the MRI Follow-up Last to Safely Identify Middle Ear Residual Cholesteatoma