CClinicalTrials.gg
CompletedNCT04886908Updated Mar 8, 2022

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

An observational study in Skin Cancer, sponsored by Brugmann University Hospital. Completed at 1 site in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-03-08.

Sponsored by Brugmann University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
373
Ages
18 Years and older
Sex
All
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Study summary

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.

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Conditions studied

  • Skin Cancer

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03

In context

Skin Neoplasms

582 studies on the registry are indexed under Skin Neoplasms; 114 are open to participants now.

This study's enrollment of 373 is above the median of 200 across 134 observational studies indexed under Skin Neoplasms.

Browse Skin Neoplasms studies →

Lead sponsor

Brugmann University Hospital is the lead sponsor of 116 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
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.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

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

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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
373 participants (actual)
Patient registry
No

Interventions

  • OtherData extraction from medical files

    Data extraction from medical files

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What researchers measure

Primary outcomes

  1. Age

    Age of the patient at the time of diagnose

    Time frame: 5 minutes

  2. Sex

    Sex of the patient

    Time frame: 5 minutes

  3. Name of the department in which the patient is followed

    Ophthalmology-CHU Brugmann hospital or Dermatology-CHU Brugmann hospital or Ophthalmology- CHU St Pierre Hospital or Dermatology-CHU St Pierre Hospital

    Time frame: 5 minutes

  4. Tumor anatomical location

    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.

    Time frame: 5 minutes

  5. Tumor size

    Tumor size in millimeters

    Time frame: 5 minutes

  6. Laterality

    Laterality: left, right, median

    Time frame: 5 minutes

  7. Multiple or single tumor

    Multiple or single tumor

    Time frame: 5 minutes

  8. Primitive tumor or recidive

    Primitive tumor or recidive

    Time frame: 5 minutes

  9. Risk factor: phototype

    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.

    Time frame: 5 minutes

  10. Risk factor: immunosuppression (yes/no)

    Pathogenic or iatrogenic, history of malignant skin tumors other than melanoma, personal or family history of melanoma

    Time frame: 5 minutes

  11. Risk factor: keratosis

    Actinic keratosis of the face

    Time frame: 5 minutes

  12. Risk factor: solar exposition (yes/no)

    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.

    Time frame: 5 minutes

  13. Diagnosis

    Time between the appearance of the tumor and the first consultation

    Time frame: 5 minutes

  14. Locoregional extension report (yes/no)

    Locoregional extension report (yes/no)

    Time frame: 5 minutes

  15. Histological diagnosis of the tumor

    Histological diagnosis of the tumor

    Time frame: 5 minutes

  16. Healthy or invaded margins

    Healthy or invaded margins

    Time frame: 5 minutes

  17. Superficial or infiltrating tumor

    Superficial or infiltrating tumor

    Time frame: 5 minutes

  18. Diagnostic method

    Diagnostic method: curettage, punch, biopsy, flattening

    Time frame: 5 minutes

  19. Surgical management method

    Biopsy resection, plasty, graft, second-line healing, enucleation, additional treatment: radiotherapy, immunotherapy, liquid nitrogen

    Time frame: 5 minutes

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Study locations

1 site
  • CHU Brugmann
    Brussels, 1020, Belgium
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 8, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04886908
Lead sponsor
Brugmann University Hospital
Responsible party
Laurence Postelmans (Head of Opthalmology clinic, Brugmann University Hospital) — Principal investigator
First posted
May 14, 2021
Start date
Feb 9, 2021
Primary completion
Jul 28, 2021
Completion
Jul 28, 2021
Last update
Mar 8, 2022

Study contacts

Nosria Boulakhrif
principal investigator · CHU Brugmann

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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