Surgery or Chemotherapy in Recurrent Ovarian Cancer (SOC 1 Trial)?
This study is currently recruiting participants.
Verified January 2013 by Shanghai Gynecologic Oncology Group
Sponsor:
Shanghai Gynecologic Oncology Group
Collaborators:
Fudan University
Zhejiang Cancer Hospital
Information provided by (Responsible Party):
Shanghai Gynecologic Oncology Group
ClinicalTrials.gov Identifier:
NCT01611766
First received: May 30, 2012
Last updated: January 2, 2013
Last verified: January 2013
| Tracking Information | |||||||||
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| First Received Date ICMJE | May 30, 2012 | ||||||||
| Last Updated Date | January 2, 2013 | ||||||||
| Start Date ICMJE | January 2011 | ||||||||
| Estimated Primary Completion Date | January 2015 (final data collection date for primary outcome measure) | ||||||||
| Current Primary Outcome Measures ICMJE |
overall survival [ Time Frame: Up to 36 months after last patient randomized ] [ Designated as safety issue: No ] | ||||||||
| Original Primary Outcome Measures ICMJE |
overall survival [ Time Frame: Up to 36 months after last patient randomized ] [ Designated as safety issue: Yes ] | ||||||||
| Change History | Complete list of historical versions of study NCT01611766 on ClinicalTrials.gov Archive Site | ||||||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
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| Current Other Outcome Measures ICMJE | Not Provided | ||||||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||||||
| Descriptive Information | |||||||||
| Brief Title ICMJE | Surgery or Chemotherapy in Recurrent Ovarian Cancer (SOC 1 Trial)? | ||||||||
| Official Title ICMJE | Evaluation of Secondary Cytoreductive Surgery in Platinum-Sensitive Recurrent Ovarian Cancer: A Phase III, Multicenter, Randomized Trial | ||||||||
| Brief Summary | The purpose of this study is to evaluate the role of secondary cytoreduction (SCR) and validate the risk model of patient selection criteria in platinum-sensitive recurrent ovarian cancer. |
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| Detailed Description | The primary objective of this study is to compare overall survival (OS) in patients with platinum-sensitive recurrent ovarian cancer with a positive SCR score randomized to secondary cytoreductive surgery followed by chemotherapy versus chemotherapy alone. |
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| Study Type ICMJE | Interventional | ||||||||
| Study Phase | Phase 3 | ||||||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
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| Condition ICMJE |
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| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status ICMJE | Recruiting | ||||||||
| Estimated Enrollment ICMJE | 420 | ||||||||
| Estimated Completion Date | December 2017 | ||||||||
| Estimated Primary Completion Date | January 2015 (final data collection date for primary outcome measure) | ||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Female | ||||||||
| Ages | 18 Years to 80 Years | ||||||||
| Accepts Healthy Volunteers | No | ||||||||
| Contacts ICMJE |
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| Location Countries ICMJE | China | ||||||||
| Administrative Information | |||||||||
| NCT Number ICMJE | NCT01611766 | ||||||||
| Other Study ID Numbers ICMJE | V02_2010_10 | ||||||||
| Has Data Monitoring Committee | Yes | ||||||||
| Responsible Party | Shanghai Gynecologic Oncology Group | ||||||||
| Study Sponsor ICMJE | Shanghai Gynecologic Oncology Group | ||||||||
| Collaborators ICMJE |
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| Investigators ICMJE |
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| Information Provided By | Shanghai Gynecologic Oncology Group | ||||||||
| Verification Date | January 2013 | ||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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