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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03900975
Other study ID # EC/2018/1164
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 25, 2018
Est. completion date July 31, 2020

Study information

Verified date November 2020
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study only women with vulvar paget disease will be included and will be analysed retrospectively. Vulvar paget disease patients are frequently treated with surgical resection of the affected tissue. During a surgical treatment surgical margins are frequently positive. Recidives are seen frequently after surgical treatment or the development of other pathologies such as vulvar carcinoma. In this study the outcome of the vulvar paget disease will be analysed and compared between the participants. It's primary goal is to create a better view on the outcome and the prognosis to prevent e.g. complications in the future.


Description:

In this study only women with vulvar paget disease will be included and will be analysed retrospectively. Vulvar paget disease patients are frequently treated with surgical resection of the affected tissue. During a surgical treatment surgical margins are frequently positive. Recidives are seen frequently after surgical treatment or the development of other pathologies such as vulvar carcinoma. In this study the outcome of the vulvar paget disease will be analysed and compared between the participants. It's primary goal is to create a better view on the outcome and the prognosis to prevent e.g. complications in the future. All the information of the patients will be gathered retrospectively from their medical file , after they gave their consent.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date July 31, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Vulvar Paget disease Exclusion Criteria: - No exclusion criteria

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium Ghent University Hospital Ghent East Flanders

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of complications after the treatment of vulvar Paget disease Number of complications after treatment Max. 10 years after treatment
Primary Type of complications after the treatment of vulvar Paget disease Type of complications after treatment Max. 10 years after treatment