- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05853315
BCC Excision Revisited
May 14, 2023 updated by: Reinhard Told, Medical University of Vienna
Long-term Results After Surgical Basal Cell Carcinoma Excision in the Eyelid Region: Revisited
To readdress basal cell carcinoma (BCC) in the periocular region to prove histologically controlled surgical treatment efficacy and to identify high-risk characteristics.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
451
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
-
-
-
Vienna, Austria, 1090
- Medical University of Vienna
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
male and female patients with periocular basal cell carcinoma
Description
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 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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
BCC Recurrence
Time Frame: mean 3-5 years
|
mean 3-5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 12, 2019
Primary Completion (Actual)
April 1, 2023
Study Completion (Actual)
May 1, 2023
Study Registration Dates
First Submitted
May 2, 2023
First Submitted That Met QC Criteria
May 2, 2023
First Posted (Actual)
May 10, 2023
Study Record Updates
Last Update Posted (Actual)
May 16, 2023
Last Update Submitted That Met QC Criteria
May 14, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1997/2019
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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