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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00637208
Other study ID # RVS-002-IL
Secondary ID MHMC grant
Status Completed
Phase N/A
First received March 9, 2008
Last updated March 14, 2008
Start date November 2007
Est. completion date March 2008

Study information

Verified date March 2008
Source Maaynei Hayesha Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Patients with varicocele in whon early prostate cancer will be found will undergo venographic embolization of both spermatic veins. The study hypothesis is that this procedure will induce a gradual regression of the prostate volume that may decrease prostate cancer cells. Close follow-up will ensure that necessary therapy will be provided if needed according to clinical criteria. Results in terms of prostate size PSA level and tumor size will be recorded.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date March 2008
Est. primary completion date March 2008
Accepts healthy volunteers No
Gender Male
Age group 45 Years to 75 Years
Eligibility Inclusion Criteria:

- Males age 45-75

- Prostate cancer

- Presence of varicocele

- No contraindication for venography

Exclusion Criteria:

- Diseases or medications which prevent interventional vascular procedures

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
venographic occlusion of spermatic veins
Through the femoral vein a catheter is inserted into the spermatic veins in succession and the veins are occluded.

Locations

Country Name City State
Israel Maaynei Hayesha Medical Center Bnei Brak

Sponsors (1)

Lead Sponsor Collaborator
Maaynei Hayesha Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety performance of the procedure. The change in tumor size and prostate cancer cells as evaluated by trans-rectal ultrasound and prostate biopsy one year Yes
Secondary The change in size of the prostate as evaluated by ultrasound Change in PSA value. Reduction of above 20% in nocturia one year
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