Skip to content

Changes in Prostate Specific Antigen Levels During Synergo Therapy-Intravesical Chemotherapy Instillations Combined With Hyperthermia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00491296
Enrollment
Unknown
Registered
2007-06-26
Start date
2007-06-30
Completion date
2007-06-30
Last updated
2008-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder Cancer

Keywords

S/P Transuretral resection of bladder tumor, Recurrent tumor after BCG Treatment

Brief summary

PURPOSE: We determined whether Synergo therapy- intravesical chemotherapy instillation combined with hyperthermia instillation is associated with elevated prostate specific antigen (PSA). MATERIALS AND METHODS: We will treat 25 consecutive patients with bladder cancer with a 6-week course of Synergo therapy, followed by cystoscopy at 6 weeks. Blood samples for PSA determination will obtain before each synergo therapy application and at cystoscopy with each patient also serving as a control. Evaluating changes in PSA level in patients undergoing treatment with Synergo delivered local hyperthermia combined with intravesical instillation of Mitomycin C for adjuvant treatment or pt. with recurrent tu of bladder post TURT with BCGtreatment.

Interventions

DEVICESYNERGO
DEVICESYNERGO-intravesical chemotherapy instillation combined with hyperthermia

Sponsors

HaEmek Medical Center, Israel
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
30 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Recurrent transitional cell carcinoma of urinary bladder post endoscopic resection * PSA Prior synergo therapy application\<10 * Normal rectal examination * Patients willing to sign informed consent according

Exclusion criteria

* History of prostate cancer * Previous history of TCC stage T2 or higher * Invasive tu of bladder * Prior pelvic radiotherapy or systemic chemotherapy * Active prostatitis * Active tuberculosis

Countries

Israel

Contacts

Primary Contactdoron perez, M.D.
perez_do@clalit.org.il+972-4-6495115

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026