- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04497337
The Superficial Lesions in the Peri-auricular Region
July 31, 2020 updated by: Mohammed Elrabie Ahmed
The Superficial Lesions in the Peri-auricular Region; Retrospective Study
Superficial lesions on and around the ear are uncommon with many differential diagnoses and different characteristic histopathologic features.
The purpose of this study was to describe a series of peri-auricular superficial lesions and characterize the distinctive types of these lesions.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Data included in this descriptive retrospective study were collected from records of 70 patients with superficial lesions around the auricle, i.e., periauricular (preauricular, auricular, and postauricular) during the period extending between 2017 and 2019, who were primarily diagnosed and operated.
Data were retrieved, reviewed, and analyzed.
The primary analysis outcome measures were patient history (age, gender, complaint, medical advice clinic, and associated medical diseases), lesions examination (site, laterality, clinical presentation, and the number of lesions).
Also, the needed investigations for diagnosis, type of intervention, postoperative patient satisfaction were evaluated.
Evaluation of the patients' follow up was done.
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Sohag, Egypt, 82524
- Sohag University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with superficial lesions around the auricle, i.e., periauricular (preauricular, auricular, and postauricular) operated during the period extending between 2017 and 2019
- Available full demographic, clinical and histopathological data
Exclusion Criteria:
- deep lesions involving parotid or parapharyngeal space
- Missed demographic, clinical and histopathological data
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
clinical and Histopathlogical types of superficial lesion around the ear
Time Frame: Cases operated between in the previous 3 years from 2017 and 2019
|
Cases operated between in the previous 3 years from 2017 and 2019
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Sohag University hospital, Nasr City, Eastern Avenue, University Street, Sohag, Egypt
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
December 12, 2019
Primary Completion (ACTUAL)
May 16, 2020
Study Completion (ACTUAL)
June 20, 2020
Study Registration Dates
First Submitted
July 27, 2020
First Submitted That Met QC Criteria
July 31, 2020
First Posted (ACTUAL)
August 4, 2020
Study Record Updates
Last Update Posted (ACTUAL)
August 4, 2020
Last Update Submitted That Met QC Criteria
July 31, 2020
Last Verified
July 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- 18630159
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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