Hemi-Ablative Prostate Brachytherapy

NACompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

July 6, 2012

Primary Completion Date

June 20, 2018

Study Completion Date

August 31, 2018

Conditions
Prostatic NeoplasmsCancer of the Prostate
Interventions
RADIATION

Hemigland focal LDR brachytherapy

The treatment is limited to the hemigland that has been diagnosed with unilateral low to intermediate risk prostate cancer by means of pre-treatment staging with mpMRI and transperineal template biopsy. The affected hemigland will be treated with iodine-125 to a prescription dose of 145Gy. Patients will be assessed at baseline and subsequently at 6 weeks, 3, 6, 9, 12,18, 24 months after treatment with PSA and EN2 measurements and validated questionnaires relating to erectile, urinary, and bowel function and general health related quality of life. mpMRI and transperineal template biopsy will be performed 24 months after treatment.

Trial Locations (1)

GU2 7XX

Royal Surrey NHS Foundation Trust, Guildford

All Listed Sponsors
lead

Royal Surrey County Hospital NHS Foundation Trust

OTHER

NCT02632669 - Hemi-Ablative Prostate Brachytherapy | Biotech Hunter | Biotech Hunter