Prospective Evaluation of a Commercially Available Hydrogel Spacer
BP-008
Clinical Protocol for the Prospective Evaluation of a Commercially Available Hydrogel Spacer
1 other identifier
observational
20
1 country
2
Brief Summary
Dosimetry efficacy evaluation of the hydrogel spacer
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Nov 2020
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 20, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 29, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
February 8, 2022
CompletedFirst Submitted
Initial submission to the registry
March 17, 2022
CompletedFirst Posted
Study publicly available on registry
April 12, 2022
CompletedSeptember 16, 2025
April 1, 2022
7 months
March 17, 2022
September 15, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Dosimetry changes
Assessment of rectal radiation exposure as compared between rectal dose volume histograms calculated for pre and post Hydrogel Injection
1 month
Secondary Outcomes (1)
Prostate to rectum spacing
1 month
Study Arms (1)
Radiation with Hydrogel Spacer
Males at least 18 years of age, who will be undergoing radiation therapy with a hydrogel spacer in place.
Interventions
Assessment of rectal dosimetry change from pre-insertion to post-insertion in subjects with prostate cancer who have undergone radiotherapy with a hydrogel spacer.
Eligibility Criteria
Prostate Cancer
You may qualify if:
- Males
- At lease 18 years of age
- Undergoing external beam or brachy radiation therapy with a hydrogel spacer
You may not qualify if:
- Invasive adenocarcinoma that is extracapsular and demonstrates posterior extension
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- BioProtectlead
Study Sites (2)
Western Radiation Oncology
Campbell, California, 95008, United States
Northern Nevada Radiation Oncology
Reno, Nevada, 89521, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 17, 2022
First Posted
April 12, 2022
Study Start
November 20, 2020
Primary Completion
June 29, 2021
Study Completion
February 8, 2022
Last Updated
September 16, 2025
Record last verified: 2022-04
Data Sharing
- IPD Sharing
- Will not share