Comparative Retrospective Analysis of Skin Tumors of the Eyelids and Face in 2 Brussels University Hospitals Over 5 Years in Dermatology or Ophthalmology

March 7, 2022 updated by: Laurence Postelmans, Brugmann University Hospital

Skin cancers are the most common of all cancers. Their incidence has increased sharply over the decades.This increase in incidence partly reflects an aging population and behavioral patterns such as repeated exposure to the sun. Indeed, exposure to UV rays is the predominant factor involved in the pathogenesis of these tumors, hence the fact that they mainly develop in photo-exposed regions such as the cephalic extremity.

The objective of this study is to provide an epidemiological analysis of tumors in the populations of both CHU Brugmann and St Pierre hospitals.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

373

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

      • Brussels, Belgium, 1020
        • CHU Brugmann

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Identification of all patients who have undergone surgical excision of benign or malignant facial and/or eyelid tumors over the past 5 years in the Dermatology and/or Ophthalmology Departments of the CHU Saint-Pierre and CHU Brugmann hospitals.

Description

Inclusion Criteria:

Final diagnosis confirmed by pathological analysis, epidemiological and clinical information available from patients.

Exclusion Criteria:

Patients who have expressed a refusal to access their medical file or incomplete data will not be taken into account.

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

  • Observational Models: Cohort
  • Time Perspectives: Retrospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Age
Time Frame: 5 minutes
Age of the patient at the time of diagnose
5 minutes
Sex
Time Frame: 5 minutes
Sex of the patient
5 minutes
Name of the department in which the patient is followed
Time Frame: 5 minutes
Ophthalmology-CHU Brugmann hospital or Dermatology-CHU Brugmann hospital or Ophthalmology- CHU St Pierre Hospital or Dermatology-CHU St Pierre Hospital
5 minutes
Tumor anatomical location
Time Frame: 5 minutes
Eyelids are distributed in their different regions: internal cantus and external cantus, upper eyelid and lower eyelid. Same for the face: ears, zygomatic, forehead, temples, cheeks, nose, upper lip, lower lip, chin, nasolabial fold, preauricular area, retroauricular area, brow bone.
5 minutes
Tumor size
Time Frame: 5 minutes
Tumor size in millimeters
5 minutes
Laterality
Time Frame: 5 minutes
Laterality: left, right, median
5 minutes
Multiple or single tumor
Time Frame: 5 minutes
Multiple or single tumor
5 minutes
Primitive tumor or recidive
Time Frame: 5 minutes
Primitive tumor or recidive
5 minutes
Risk factor: phototype
Time Frame: 5 minutes
Phototype 1 to 6 on the Fitzpatrick scale. The Fitzpatrick scale is a numerical classification schema for human skin color. Type 1 is pale skin that always burns, never tans and type 6 is deeply pigmented dark brown to darkest brown skin that never burns.
5 minutes
Risk factor: immunosuppression (yes/no)
Time Frame: 5 minutes
Pathogenic or iatrogenic, history of malignant skin tumors other than melanoma, personal or family history of melanoma
5 minutes
Risk factor: keratosis
Time Frame: 5 minutes
Actinic keratosis of the face
5 minutes
Risk factor: solar exposition (yes/no)
Time Frame: 5 minutes
Lived in a sunny European country> 1 year, lived in a sunny country outside Europe> 1 year, sunbed use> 1 session, history of solar erythema during childhood.
5 minutes
Diagnosis
Time Frame: 5 minutes
Time between the appearance of the tumor and the first consultation
5 minutes
Locoregional extension report (yes/no)
Time Frame: 5 minutes
Locoregional extension report (yes/no)
5 minutes
Histological diagnosis of the tumor
Time Frame: 5 minutes
Histological diagnosis of the tumor
5 minutes
Healthy or invaded margins
Time Frame: 5 minutes
Healthy or invaded margins
5 minutes
Superficial or infiltrating tumor
Time Frame: 5 minutes
Superficial or infiltrating tumor
5 minutes
Diagnostic method
Time Frame: 5 minutes
Diagnostic method: curettage, punch, biopsy, flattening
5 minutes
Surgical management method
Time Frame: 5 minutes
Biopsy resection, plasty, graft, second-line healing, enucleation, additional treatment: radiotherapy, immunotherapy, liquid nitrogen
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nosria Boulakhrif, CHU Brugmann

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)

February 9, 2021

Primary Completion (Actual)

July 28, 2021

Study Completion (Actual)

July 28, 2021

Study Registration Dates

First Submitted

May 6, 2021

First Submitted That Met QC Criteria

May 10, 2021

First Posted (Actual)

May 14, 2021

Study Record Updates

Last Update Posted (Actual)

March 8, 2022

Last Update Submitted That Met QC Criteria

March 7, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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.

Clinical Trials on Skin Cancer

Clinical Trials on Data extraction from medical files

3
Subscribe