Quality of Life After Permanent Interstitial Iodine Seed Prostate Brachytherapy

NCT ID: NCT02652000

Last Updated: 2016-12-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-10-31

Study Completion Date

2016-12-31

Brief Summary

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Retrospective study to analyze Quality of life in men after iodine seed brachytherapy for localized prostate cancer

Detailed Description

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Retrospective Evaluation of Quality of life data collected on men who underwent iodine seed brachytherapy at the University Hospital Zurich

Conditions

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Neoplasms, Prostate

Study Design

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Study Time Perspective

RETROSPECTIVE

Interventions

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No intervention in this retrospective study

No Intervention in this retrospective Analysis.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male \> 18 years of age
* iodine seed brachytherapy for localized prostate cancer at the University Hospital Zurich

Exclusion Criteria

* No iodine seed brachytherapy for localized prostate cancer at the University Hospital Zurich
Minimum Eligible Age

48 Years

Maximum Eligible Age

80 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role collaborator

Kantonsspital Graubuenden

OTHER

Sponsor Role lead

Responsible Party

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Daniel Rudolf Zwahlen

MD, MBA

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Daniel R Zwahlen, MD, MBA

Role: PRINCIPAL_INVESTIGATOR

Kantonsspital Graubuenden

Locations

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Kantonsspital Graubuenden, Department of Radiaton Oncology

Chur, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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KEK-ZH-Nr. 2015-0573

Identifier Type: -

Identifier Source: org_study_id