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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00213694
Other study ID # 2003/052/HP
Secondary ID
Status Completed
Phase Phase 2
First received September 13, 2005
Last updated March 4, 2013
Start date November 2003
Est. completion date June 2006

Study information

Verified date March 2013
Source University Hospital, Rouen
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

Clinical response to chemotherapy. Biological parameter (PSA) and RECIST evaluation. Association of Docetaxel (J 15) and Celecoxib.


Description:

Association Docetaxel (J 15) and celecoxib Patient survival Biological parameter : PSA Clinical status RECIST evaluation


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date June 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria:

- metastatic prostate cancer

- ASCO progression criteria

Exclusion Criteria:

- other prostate chemotherapy

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Drug:
docetaxel and celecoxib


Locations

Country Name City State
France Charles Nicolle, University Hospital Rouen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Rouen

Country where clinical trial is conducted

France, 

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