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Spots Global Cancer Trial Database for Study Comparing Weekly Versus Every 3 Week Chemotherapy in Patients With Ovarian Cancer

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Trial Identification

Brief Title: Study Comparing Weekly Versus Every 3 Week Chemotherapy in Patients With Ovarian Cancer

Official Title: Weekly Versus Every 3 Week Carboplatin and Paclitaxel in Patients With Ovarian Cancer: a Phase III Randomized Multicenter Study

Study ID: NCT00660842

Conditions

Ovarian Cancer

Study Description

Brief Summary: The purpose of this study is to study efficacy and the effects on quality of life in women with ovarian cancer treated with a weekly schedule of chemotherapy with carboplatin and paclitaxel compared to those treated with standard every 3 weeks schedule of the same chemotherapy.

Detailed Description: The standard first-line treatment of ovarian cancer is combination chemotherapy with carboplatin and paclitaxel, given every 3 weeks. Researchers are looking at new ways of giving chemotherapy to make it more tolerable and more effective. One way is by giving the chemotherapy more often in smaller doses. This approach can be associated with fewer or less troubling side effects. Some chemotherapy drugs such as paclitaxel have been shown to also be more active when given once a week rather than once every 3 week schedule.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

IRCCS Oncologico Bari, Oncologia Medica, Bari, BA, Italy

Ospedale Riuniti di Bergamo, U.O. di Ostetricia e Ginecologia, Bergamo, BG, Italy

Ospedale Fatebenefratelli, U.O. di Oncologia, Benevento, BN, Italy

Azienda Ospedaliera G. Rummo, Benevento, BN, Italy

Università Cattolica del Sacro Cuore, Dipartimento di Oncologia, Campobasso, CB, Italy

Azienda Ospedaliera C. Poma, Mantova, MN, Italy

Azienda Ospedaliera V. Cervello, Palermo, PA, Italy

Ospedale S. Massimo, Day Hospital Oncologico, Penne, PE, Italy

Centro di Riferimento Oncologico, Divisione di Oncolgia Medica C, Aviano, PN, Italy

Ospedale S. Chiara, Trento, TN, Italy

Ospedale S. Bortolo ULSS 6, U.O. di Oncologia Medica, Vicenza, VI, Italy

Ospedale Mazzoni, Ascoli Piceno, , Italy

Policlinico Universitario, Bari, , Italy

Universita di Bari Policinico I Clinical Ostetrica e Ginecologica, Bari, , Italy

Ospedale Fatebenefratelli, Benevento, , Italy

Ospedale Senatore Antonio Perrino, Brindisi, , Italy

Universita Cattolica del Sacro Cuore, Campobasso, , Italy

Ospedale A. Manzoni, Lecco, , Italy

Istituto Nazionale Tumori, Milano, , Italy

A.O. Univeristaria Policlinico, Modena, , Italy

Azienda Ospedaliera D. Cotugno, Napoli, , Italy

Istituto Nazionale dei Tumori , Oncologia Medica - Dipartimento Uro-Ginecologico, Napoli, , Italy

Università Federico II, Cattedra di Oncologia Medica, Napoli, , Italy

Ospedale Silvestrini, Perugia, , Italy

Ospedale Civile S. Spirito, Pescara, , Italy

A.O. S. Maria degli Angeli, Pordenone, , Italy

Ospedale S. Giovanni Calibita Fatebenefratelli, UO di Oncologia, Roma, , Italy

A.O. di Udine S. Maria della Misericordia, Udine, , Italy

Contact Details

Name: Sandro Pignata, M.D., Ph.D.

Affiliation: National Cancer Institute, Naples

Role: PRINCIPAL_INVESTIGATOR

Name: Francesco Perrone, M.D., Ph.D.

Affiliation: National Cancer Institute, Naples

Role: PRINCIPAL_INVESTIGATOR

Name: Marilina Piccirillo, M.D.,

Affiliation: National Cancer Institute, Naples

Role: PRINCIPAL_INVESTIGATOR

Name: Ciro Gallo, M.D., Ph.D.

Affiliation: University of Campania "Luigi Vanvitelli"

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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