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Clinical Trials/EUCTR2005-005967-27-IT
EUCTR2005-005967-27-IT
Active, not recruiting
Not Applicable

Study pilot of metronomic chemotherapy with ciclofosfamide, celecoxib and desametasone in patients with diagnosis of carcinoma of the refractory ormon prostate in advanced stage appraisal pharmacodynamics - PROMET

AZIENDA USL 6 LIVORNO ZONA LIVORNESE0 sites27 target enrollmentFebruary 17, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ORMONO REFRACTORY CARCINOMA OF PROSTATE IN ADVANCED STAGE
Sponsor
AZIENDA USL 6 LIVORNO ZONA LIVORNESE
Enrollment
27
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 17, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Male

Investigators

Sponsor
AZIENDA USL 6 LIVORNO ZONA LIVORNESE

Eligibility Criteria

Inclusion Criteria

  • Patients with diagnosis of ormonorefrattario prostatico carcinoma in advanced phase \- ECOG PS 2 \- Attended of life at least 3 months \- Adapted renal functionality creatinina 1,25 x V.N. \- Adapted hepatic functionality bilirubina tot. 1,5 x V.N., SGOT and SGPT 3 xV.N., \- Adapted reservoir medullary GB 3000/mcl, PLT 100\.000/mcl, Hgb 10 g/dl. \- informed Consent written \- Suspension from at least 30 drug days antiandrogens with demonstration not answer of the PSA to the suspension
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) no
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • Scompensate metabolic diseases or serious infections in action \- cardiac Arrhythmies or ischemic cardiopathy and presence of whichever elevated cardiovascular risk \- Impossibility to execute adequate follow\-up \- Presence of sintomatic encefalic metastases \- a Presence of second neoplasia. \- gastroduodenal Presence of ulcera

Outcomes

Primary Outcomes

Not specified

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