Prostate Cancer Clinical Trial

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Prospective Evaluation of a Commercially Available Hydrogel Spacer

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Summary

Dosimetry efficacy evaluation of the hydrogel spacer

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Full Description

Single arm study for evaluation of dosimetry following use of a commercially available hydrogel spacer implanted in 20 males undergoing radiotherapy to treat prostate cancer. Study will utilize pre and post gel insertion CT images to determine the endpoints.

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Eligibility Criteria

Inclusion Criteria:

Males
At lease 18 years of age
Undergoing external beam or brachy radiation therapy with a hydrogel spacer

Exclusion Criteria:

Invasive adenocarcinoma that is extracapsular and demonstrates posterior extension

Study is for people with:

Prostate Cancer

Estimated Enrollment:

20

Study ID:

NCT05323747

Recruitment Status:

Completed

Sponsor:

BioProtect

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There are 2 Locations for this study

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Western Radiation Oncology
Campbell California, 95008, United States
Northern Nevada Radiation Oncology
Reno Nevada, 89521, United States

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Estimated Enrollment:

20

Study ID:

NCT05323747

Recruitment Status:

Completed

Sponsor:


BioProtect

How clear is this clinincal trial information?

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