Clinical Trial: CRP On Radiobiological and Clinical Study On Virally-Induced Cancers Response to Radiotherapy

This study is not yet open for patient recruitment.

Sponsored by: International Atomic Energy Agency
Information provided by: International Atomic Energy Agency

Purpose

To study clinical effects of two/four HDR brachytherapy applications and teletherapy with or without weekly Cisplatin in cervix cancer.
Condition Intervention Phase
Cervix Cancer
 Procedure: Radiotherapy alone and Radiotherapy with Cisplatin
Phase III

MedlinePlus related topics:  Cervical Cancer

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Female
Criteria

Inclusion Criteria:

  • Cervix Cancer

Exclusion Criteria:

  • unable to give an informed consent

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00122772

Branislav Jeremic, M.D., Ph.D.      +43-1-2600  Ext. 21666    B.Jeremic@iaea.org

Study chairs or principal investigators

Branislav Jeremic, M.D., Ph.D.,  Study Director,  International Atomic Energy Agency (IAEA)   

More Information

Study ID Numbers:  E33024
Record last reviewed:  July 2005
Last Updated:  July 25, 2005
Record first received:  July 21, 2005
ClinicalTrials.gov Identifier:  NCT00122772
Health Authority: United Nations: International Atomic Energy Agency
ClinicalTrials.gov processed this record on 2005-07-26

Resources

  • CRP (Lab Tests Online)



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