Health Condition 1: null- CA OVARY
Conditions
Interventions
Intervention1: Routine Lymphadenectomy: Patients undergoing interval debulking
Control Intervention1: No lymphadenectomy: Patients undergoing interval debulking
Sponsors
IRB CMCH Vellore
Eligibility
Inclusion criteria
Inclusion criteria: Patients who have undergone neoadjuvant chemotherapy for primary ovarian cancer or PPC followed by optimal interval debulking
Exclusion criteria
Exclusion criteria: Sub-optimal debulking, poor performance status
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the morbidity and mortality associated with pelvic & para-aortic lymphadenectomy in patients with epithelial ovarian cancer who undergo interval debulking (after chemotherapy)Timepoint: Immediate Post OP and then at 3 month intervals | — |
Secondary
| Measure | Time frame |
|---|---|
| Progression free survival and overall survivalTimepoint: At the end of 3 years and 5 years | — |
Countries
India
Contacts
Public ContactAbraham Peedicayil
CMCH
Outcome results
None listed