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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04795297
Other study ID # RECHMPL21_0156
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date February 20, 2021

Study information

Verified date March 2021
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

.During one year all the resected basal cell carcinomas (BCC) analyzed in Montpellier University Hospital Anatomopathology unit were included in this study. Localisation and histological characteristics were collected. All the recurrences of BCC were searched from the medical records (or histopathology request form). From 804 BCC, 48 were recurrent BCC with or without complete first resection. Patients with recurrent BCC were contacted to obtain agreement and more informations about the first resection and some clinical informations like sun exposure and phototype. The statistical analysis focused on the localisation of recurrent BCC (with a complete first resection) compared to localisations of primary BCC in this population. The goal was to identified localisations with an increased risk of recurrences.


Recruitment information / eligibility

Status Completed
Enrollment 804
Est. completion date February 20, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 99 Years
Eligibility Cohort : Inclusion criteria: - Patients with resected BCC Exclusion criteria: - Biopsies of BCC, - revised surgery of incomplete resection. Cases : Inclusion criteria: -Recurrent BCC with complete first resection Exclusion criteria: - Recurrent BCC with incomplete first resection, Patients with Gorlin syndrome (a genetic disease that increase risk of BCC)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary - Determined For each localisation the number of primary and recurrent BCC and analysis of localisation with higher risk of BCC - Determined For each localisation the number of primary and recurrent BCC and analysis of localisation with higher risk of BCC 1 day
Secondary Analysis of correlation between localisation and histology characteristics Analysis of correlation between localisation and histology characteristics 1 day
Secondary Analysis of correlation between histological type and recurrence risk Analysis of correlation between histological type and recurrence risk 1 day
Secondary Analysis if there is a difference between first resection histological type and the recurrent histological type Analysis if there is a difference between first resection histological type and the recurrent histological type 1 day
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