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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05733728
Other study ID # 1942/2022
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 23, 2023
Est. completion date December 31, 2030

Study information

Verified date May 2023
Source Medical University of Vienna
Contact Reinhard Told
Phone +4314040048470
Email reinhard.told@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Background: Uveal melanoma (UM) is a common primary ocular malignancy associated with limited overall survival in the advanced stage of the disease. Fundamental breakthrough regarding the management of the disease and the overall-survival have not yet been achieved. Studies with large cohorts are difficult to perform due to limited patient numbers, therefore retrospective analyses are of great potential to gain further knowledge in a disease with high clinical needs. Aim: The proposed project is a register for patients with UM treated at the Department of Ophthalmology and Optometry at the Medical University of Vienna between 01.01.1997 and 31.12.2021. Patients and Methods: Patients treated for UM at the Department of Ophthalmology and Optometry at the Medical University of Vienna between 01.01.1997 and 31.12.2021 will be included in the register. Information on the baseline characteristics, survival times and course of the disease will be gathered via retrospective chart review and saved in a password-secured database.


Recruitment information / eligibility

Status Recruiting
Enrollment 1400
Est. completion date December 31, 2030
Est. primary completion date December 31, 2030
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria - Patients 18 - 99 years - Diagnosis of uveal melanoma Exclusion Criteria - Patients younger than 18 years of age - Inadequate or missing information on the clinical course in patient charts

Study Design


Related Conditions & MeSH terms


Intervention

Other:
any therapy suitable
any therapy suitable

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 Conduction of a Register providing the basis for Retrospective studies analyzing the obtained data and easy identification of patients for prospective studies (e.g. long-term survival analysis) 1997-2021
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