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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00130858
Other study ID # CWS-IV 2002
Secondary ID
Status Completed
Phase Phase 2
First received August 15, 2005
Last updated April 1, 2009
Start date January 2005
Est. completion date March 2009

Study information

Verified date April 2009
Source Cooperative Weichteilsarkom Study Group
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Interventional

Clinical Trial Summary

Phase II Study to evaluate the response on two blocks of topotecan and carboplatin


Description:

Phase II study for patients with chemosensible soft tissue sarcoma stage IV in children and adolescents ; response according to RECIST criteria following two blocks of combination therapy consisting of Topotecan and carboplatin


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date March 2009
Est. primary completion date December 2007
Accepts healthy volunteers No
Gender Both
Age group N/A to 21 Years
Eligibility Inclusion Criteria:

- Soft tissue sarcoma chemosensible, stage IV

- age < 21

- measurable tumor lesions

Exclusion Criteria:

- Lack of cooperation by the patient

- no willingness of follow-up examinations

- participation on another clinical trial at the same time

- death due to the sickness within four weeks

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Topotecan

Carboplatin


Locations

Country Name City State
Germany Zentralklinikum Augsburg
Germany Klinikum Berlin-Buch Berlin
Germany Virchow Klinik Berlin
Germany Zentrum für Kinderheilkunde Bonn
Germany Zentralkrankenhaus Bremen Bremen
Germany Universitätsklinik der technischen Universität Dresden Dresden
Germany Heinrich-Heine-Universität Düsseldorf
Germany HELIOS Klinikum Erfurt GmbH Erfurt Sachsen
Germany Universitätsklinik für Kinderund Jugendliche Erlangen
Germany Universitätsklinikum Essen Essen
Germany Klinikum der Universität Frankfurt
Germany Universitäts-Kinderklinik Freiburg Freiburg
Germany Klinikum der Justus-Liebig-Universität Gießen
Germany Georg-August-Universität Göttingen
Germany Universitäts-Kinderklinik Hamburg Hamburg
Germany Kinderklinik der Medizinischen Hochschule Hannover
Germany Universitäts-Kinderklinik Heidelberg
Germany Universitäts-Kinderklinik Homburg/saar
Germany Klinik für Kinder- und Jugendmedizin Jena
Germany Städtisches Klinikum Karlruhe Karlsruhe
Germany Klinikum der Universität Kiel Kiel
Germany Klinikum der Stadt Köln Köln
Germany Universitäts-Kinderklinik Köln
Germany Universitätsklinik und Poliklinik Leipzig
Germany Medizinische Universität zu Lübeck Lübeck
Germany Kinderklinik St. Annastift Ludwigshafen
Germany Medizinische Fakultät Magdeburg
Germany Klinikum der Johannes-Gutenberg-Universität Mainz
Germany Dr. von Haunersches Kinderspital München
Germany Städtisches Krankenhaus Technische Universität Schwabing München
Germany Westfälische Wilhelms-Universität Münster
Germany Cnopf'sche Kinderklinik Nürnberg
Germany Klinik St. Hedwig Regensburg
Germany Johanniter-Kinderklinik St.Augustin
Germany Olgahospital Stuttgart
Germany Universitäts-Kinderklinik Tübingen
Germany Universitäts-Kinderklinik Ulm
Germany Universitäts-Kinderklinik Würzburg

Sponsors (2)

Lead Sponsor Collaborator
Cooperative Weichteilsarkom Study Group Deutsche Krebshilfe e.V., Bonn (Germany)

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response according to RECIST criteria
Secondary Toxicity
Secondary Overall-Survival
Secondary Event-free-survival
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