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Clinical Trials/NCT02717936
NCT02717936
Unknown
N/A

Prospektive Therapie-Studie Zur Behandlung Des Desmoplastischen Plattenepithelkarzinoms

University Hospital Tuebingen1 site in 1 country73 target enrollmentJanuary 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Squamous Cell Carcinoma of the Skin
Sponsor
University Hospital Tuebingen
Enrollment
73
Locations
1
Primary Endpoint
Recurrence free survival of patients with desmoplastic squamous cell carcinoma (SCC) diagnosed with immunohistochemistry .
Last Updated
10 years ago

Overview

Brief Summary

Aim of the study is to verify wether it is possible to have a more sensitive diagnostic tool using pancytokeratin immunohistochemistry for desmoplastic squamous cell carcinoma compared to regular H&E staining. The investigators therefore plan to include 73 participants with a confirmed diagnosis of desmoplastic squamous cell carcinoma and do regular follow up.

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
January 2020
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • desmoplastic squamous cell carcinoma (SCC) of the skin

Exclusion Criteria

  • tumor recurrence
  • collision tumors
  • other skin malignancies
  • Rothmund-Thomson-Syndrome
  • lacking of the capacity for informed consent

Outcomes

Primary Outcomes

Recurrence free survival of patients with desmoplastic squamous cell carcinoma (SCC) diagnosed with immunohistochemistry .

Time Frame: 4 years

Secondary Outcomes

  • Presence of perineurial and perivascular tumor invasion according to histological work-up(4 years)
  • Dimension of the tumor spreading according to histological work-up (measured in mm)(4 years)
  • Histological pattern of tumour growth (continuous versus discontinuous)(4 years)
  • Reduction of local recurrence with immunohistochemistry(4 years)

Study Sites (1)

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