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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05853315
Other study ID # 1997/2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 12, 2019
Est. completion date May 1, 2023

Study information

Verified date May 2023
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To readdress basal cell carcinoma (BCC) in the periocular region to prove histologically controlled surgical treatment efficacy and to identify high-risk characteristics.


Recruitment information / eligibility

Status Completed
Enrollment 451
Est. completion date May 1, 2023
Est. primary completion date April 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria: - Patient records were reviewed for the presence of BCC and surgical excision with frozen sections control of the wound margins in the periocular region, - conducted between 01.01.2009 and 31.12.2019. - Periocular was defined as the area involving the medial and lateral canthus as well as the upper and lower eyelids. Exclusion criteria: - BCCs outside of this region were excluded from this analysis, - as well as incomplete records.

Study Design


Intervention

Procedure:
Surgery
Surgical Excision

Locations

Country Name City State
Austria Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary BCC Recurrence mean 3-5 years
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