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Spots Global Cancer Trial Database for Post-marketing Surveillance Regarding Efficacy and Safety of SpaceOAR™

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Post-marketing Surveillance Regarding Efficacy and Safety of SpaceOAR™

Official Title: Prospective National Post-marketing Surveillance for the Investigation of the Efficacy and Safety of SpaceOAR™ to Maintain Space Between the Rectum and Prostate During Radiation Therapy

Study ID: NCT01999660

Study Description

Brief Summary: A treatment with SpaceOAR™ hydrogel does reduce late toxicity Grad 2 and Grad 3 of radiation therapy in prostate cancer patients

Detailed Description: The degradable SpaceOAR™ hydrogel establishes for the time of radiotherapy a distance between the prostate and the rectum

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Clinic for Radiooncology and Radiotherapy, Evangelical Clinics Gelsenkirchen, Gelsenkirchen, NRW, Germany

Contact Details

Name: Razvan Galalae, PD Dr. med.

Affiliation: Clinic for Radiooncology and Radiotherapy, Evangelical Clinics Gelsenkirchen, Germany

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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